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                            {
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                "minor_allelic_frequency": "",
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                            {
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                            {
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                            {
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                                "id": "MONDO:0009656",
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                            {
                                "id": "MONDO:0009656",
                                "resource": "MONDO",
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                                "url": "https://www.omim.org/entry/252920",
                                "name": "Mucopolysaccharidosis 3B",
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            },
            {
                "evidence": [
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                    {
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                "sequence_mut": "M",
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                            {
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                            {
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                                "url": "https://monarchinitiative.org/disease/MONDO:0014665",
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                                "description": "Any Charcot-Marie-Tooth disease in which the cause of the disease is a mutation in the NAGLU gene."
                            },
                            {
                                "id": "MONDO:0014665",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0014665",
                                "name": "CMT2V",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0014665",
                                "resource": "MONDO",
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                                "name": "Charcot-Marie-Tooth disease caused by mutation in NAGLU",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0014665",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0014665",
                                "name": "Charcot-Marie-Tooth neuropathy type 2V",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0014665",
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                                "url": "https://monarchinitiative.org/disease/MONDO:0014665",
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                            },
                            {
                                "id": "MONDO:0014665",
                                "resource": "MONDO",
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                                "name": "autosomal dominant Charcot-Marie-Tooth disease type 2 due to NAGLU mutation",
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                            },
                            {
                                "id": "MONDO:0014665",
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                                "name": "autosomal dominant Charcot-Marie-Tooth disease type 2V",
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                            {
                                "id": "MONDO:0014665",
                                "resource": "MONDO",
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                                "name": "autosomal dominant axonal Charcot-Marie-Tooth disease type 2V",
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                            {
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                                "id": "MONDO:0009656",
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                            {
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                                "id": "MONDO:0009656",
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                            {
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                                "id": "DOID:0110178",
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                            {
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                            {
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                            {
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                            {
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                            {
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                            },
                            {
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                            },
                            {
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                            {
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                            },
                            {
                                "id": "MONDO:0009656",
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                            {
                                "id": "MONDO:0009656",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009656",
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                                "description": ""
                            },
                            {
                                "id": "MONDO:0009656",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009656",
                                "name": "Sanfilippo syndrome type B",
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                            {
                                "id": "MONDO:0009656",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009656",
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                            {
                                "id": "MONDO:0009656",
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                                "description": ""
                            },
                            {
                                "id": "DOID:0110178",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0110178",
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                            {
                                "id": "DOID:0110178",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0110178",
                                "name": "autosomal dominant axonal Charcot-Marie-Tooth disease type 2V",
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                            {
                                "id": "MONDO:0014665",
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                            {
                                "id": "MONDO:0014665",
                                "resource": "MONDO",
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                                "name": "Charcot-Marie-Tooth disease caused by mutation in NAGLU",
                                "description": ""
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                            {
                                "id": "MONDO:0014665",
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                                "url": "https://monarchinitiative.org/disease/MONDO:0014665",
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                            },
                            {
                                "id": "MONDO:0014665",
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                            {
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                            },
                            {
                                "id": "MONDO:0014665",
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                            {
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                                "name": "Mucopoly-saccharidosis type 3B",
                                "description": ""
                            },
                            {
                                "id": "DOID:0111394",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0111394",
                                "name": "Mucopolysaccharidosis type 3B",
                                "description": ""
                            },
                            {
                                "id": "DOID:0111394",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0111394",
                                "name": "N-acetyl-alpha-glucosaminidase deficiency",
                                "description": ""
                            },
                            {
                                "id": "DOID:0111394",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0111394",
                                "name": "NAGLU deficiency",
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                            },
                            {
                                "id": "DOID:0111394",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0111394",
                                "name": "Sanfilippo syndrome type B",
                                "description": ""
                            },
                            {
                                "id": "DOID:0111394",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0111394",
                                "name": "mucopolysaccharidosis type IIIB (Sanfilippo B)",
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                            },
                            {
                                "id": "MONDO:0009656",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009656",
                                "name": "mucopolysaccharidosis type 3B",
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                            },
                            {
                                "id": "MONDO:0009656",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009656",
                                "name": "MPS III B",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009656",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009656",
                                "name": "MPS3B",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009656",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009656",
                                "name": "MPSIIIB",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009656",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009656",
                                "name": "N-acetyl-alpha-glucosaminidase deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009656",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009656",
                                "name": "Sanfilippo B",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009656",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009656",
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                                "description": ""
                            },
                            {
                                "id": "MONDO:0009656",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009656",
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                            },
                            {
                                "id": "MONDO:0009656",
                                "resource": "MONDO",
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                                "description": ""
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                            {
                                "id": "MONDO:0009656",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009656",
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                            {
                                "id": "MONDO:0009656",
                                "resource": "MONDO",
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                            {
                                "id": "MONDO:0009656",
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                                "description": ""
                            },
                            {
                                "id": "MONDO:0009656",
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                            },
                            {
                                "id": "MONDO:0009656",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009656",
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                            },
                            {
                                "id": "MONDO:0009656",
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                                "id": "MONDO:0009656",
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                            },
                            {
                                "id": "MONDO:0009656",
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                            {
                                "id": "MONDO:0009656",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009656",
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                                "description": ""
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                            {
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                                "resource": "MIM",
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                            {
                                "id": "0009656",
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                                "url": "https://monarchinitiative.org/disease/MONDO:0009656"
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                            {
                                "id": "252920",
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                        ]
                    },
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                                "id": "DOID:0111394",
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                                "id": "DOID:0111394",
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                                "id": "DOID:0111394",
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                                "url": "http://disease-ontology.org/term/DOID:0111394",
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                                "id": "DOID:0111394",
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                                "id": "DOID:0111394",
                                "resource": "Disease Ontology",
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                            },
                            {
                                "id": "DOID:0111394",
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                            {
                                "id": "DOID:0111394",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0111394",
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                                "url": "https://monarchinitiative.org/disease/MONDO:0009656",
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                            {
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                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009656",
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                            },
                            {
                                "id": "MONDO:0009656",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009656",
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                            {
                                "id": "MONDO:0009656",
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                            {
                                "id": "MONDO:0009656",
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                            {
                                "id": "MONDO:0009656",
                                "resource": "MONDO",
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                            {
                                "id": "MONDO:0009656",
                                "resource": "MONDO",
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                            {
                                "id": "MONDO:0009656",
                                "resource": "MONDO",
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                            {
                                "id": "MONDO:0009656",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009656",
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                            {
                                "id": "MONDO:0009656",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009656",
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                            {
                                "id": "MONDO:0009656",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009656",
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                            {
                                "id": "MONDO:0009656",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009656",
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                                "description": ""
                            },
                            {
                                "id": "MONDO:0009656",
                                "resource": "MONDO",
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                            {
                                "id": "MONDO:0009656",
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                                "url": "https://monarchinitiative.org/disease/MONDO:0009656",
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                            {
                                "id": "MONDO:0009656",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009656",
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                            {
                                "id": "MONDO:0009656",
                                "resource": "MONDO",
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                            {
                                "id": "MONDO:0009656",
                                "resource": "MONDO",
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                            {
                                "id": "MONDO:0009656",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009656",
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                                "url": "https://monarchinitiative.org/disease/MONDO:0009656"
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                            {
                                "id": "252920",
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            },
            {
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            {
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                            {
                                "id": "DOID:4159",
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                                "id": "DOID:4159",
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                            }
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            {
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                                "resource": "Disease Ontology",
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                            {
                                "id": "DOID:0110178",
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                            {
                                "id": "DOID:0110178",
                                "resource": "Disease Ontology",
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                            {
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                                "url": "http://disease-ontology.org/term/DOID:0110178",
                                "name": "autosomal dominant axonal Charcot-Marie-Tooth disease type 2V",
                                "description": ""
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                            {
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                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0014665",
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                            },
                            {
                                "id": "MONDO:0014665",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0014665",
                                "name": "CMT2V",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0014665",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0014665",
                                "name": "Charcot-Marie-Tooth disease caused by mutation in NAGLU",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0014665",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0014665",
                                "name": "Charcot-Marie-Tooth neuropathy type 2V",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0014665",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0014665",
                                "name": "NAGLU Charcot-Marie-Tooth disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0014665",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0014665",
                                "name": "autosomal dominant Charcot-Marie-Tooth disease type 2 due to NAGLU mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0014665",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0014665",
                                "name": "autosomal dominant Charcot-Marie-Tooth disease type 2V",
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                            },
                            {
                                "id": "MONDO:0009656",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009656",
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                            },
                            {
                                "id": "MONDO:0009656",
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                            {
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                                "resource": "MONDO",
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                            },
                            {
                                "id": "MONDO:0009656",
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                                "url": "https://monarchinitiative.org/disease/MONDO:0009656",
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                                "description": ""
                            },
                            {
                                "id": "MONDO:0009656",
                                "resource": "MONDO",
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                            },
                            {
                                "id": "MONDO:0009656",
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                            {
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                            },
                            {
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                            {
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                            {
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                            {
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                "glycoeffect": [],
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                "end_pos": 74,
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                "sequence_mut": "null",
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                "chr_pos": "42536492",
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                "minor_allelic_frequency": "",
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                            {
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                            {
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                            {
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                            {
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                            {
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                            {
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                                "url": "http://disease-ontology.org/term/DOID:0111394",
                                "name": "NAGLU deficiency",
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                                "id": "DOID:0111394",
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                                "id": "DOID:0111394",
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                            {
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                            {
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                            {
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                            {
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                            {
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                            {
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                            {
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                            {
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                                "url": "https://monarchinitiative.org/disease/MONDO:0014665",
                                "name": "Charcot-Marie-Tooth neuropathy type 2V",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0014665",
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                                "url": "https://monarchinitiative.org/disease/MONDO:0014665",
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                                "id": "MONDO:0014665",
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                                "id": "MONDO:0014665",
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                            {
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                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/252920",
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                                "id": "252920",
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                                "id": "DOID:0110178",
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                            {
                                "id": "DOID:0110178",
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                            {
                                "id": "MONDO:0014665",
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                            {
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                            {
                                "id": "MONDO:0014665",
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                            {
                                "id": "MONDO:0014665",
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                            {
                                "id": "MONDO:0014665",
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                                "id": "MONDO:0014665",
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                            {
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                            {
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                            {
                                "id": "MONDO:0009656",
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                            {
                                "id": "MONDO:0009656",
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                            {
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                            {
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                                "id": "MONDO:0009656",
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                            {
                                "id": "MONDO:0009656",
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                            {
                                "id": "MONDO:0009656",
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                            {
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                            {
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                            {
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                            {
                                "id": "MONDO:0009656",
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                            {
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                            {
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            },
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                            {
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                            {
                                "id": "MONDO:0014665",
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                            {
                                "id": "MONDO:0014665",
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                    {
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                            "name": "Charcot-Marie-Tooth disease axonal type 2V",
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                                "id": "DOID:0110178",
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                            {
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                            {
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                            {
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                            {
                                "id": "MONDO:0009656",
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                            {
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                            {
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                                "id": "MONDO:0014665",
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                            {
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                            {
                                "id": "MONDO:0014665",
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                            {
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                            {
                                "id": "MONDO:0014665",
                                "resource": "MONDO",
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                            {
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                            {
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                            {
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                                "url": "http://disease-ontology.org/term/DOID:0111394",
                                "name": "mucopolysaccharidosis type IIIB (Sanfilippo B)",
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                            {
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                            {
                                "id": "MONDO:0009656",
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                            {
                                "id": "MONDO:0009656",
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                            {
                                "id": "MONDO:0009656",
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                            },
                            {
                                "id": "MONDO:0009656",
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                            {
                                "id": "MONDO:0009656",
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                            {
                                "id": "MONDO:0009656",
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                            {
                                "id": "MONDO:0009656",
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                            {
                                "id": "MONDO:0009656",
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                            {
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                            {
                                "id": "MONDO:0009656",
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                            {
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                                "id": "MONDO:0009656",
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                            {
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                            {
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                "minor_allelic_frequency": "",
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                                "id": "MONDO:0009656",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009656",
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                                "description": ""
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                            {
                                "id": "MONDO:0009656",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009656",
                                "name": "MPSIIIB",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009656",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009656",
                                "name": "N-acetyl-alpha-glucosaminidase deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009656",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009656",
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                                "description": ""
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                            {
                                "id": "MONDO:0009656",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009656",
                                "name": "Sanfilippo syndrome B",
                                "description": ""
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                            {
                                "id": "MONDO:0009656",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009656",
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                                "description": ""
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                            {
                                "id": "MONDO:0009656",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009656",
                                "name": "mucopolysaccharidosis type 3B",
                                "description": ""
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                            {
                                "id": "MONDO:0009656",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009656",
                                "name": "mucopolysaccharidosis type IIIB",
                                "description": ""
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                            {
                                "id": "MONDO:0009656",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009656",
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                            {
                                "id": "MONDO:0009656",
                                "resource": "MONDO",
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                                "resource": "MONDO",
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                                "id": "MONDO:0009656",
                                "resource": "MONDO",
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                            {
                                "id": "MONDO:0009656",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009656",
                                "name": "N-Acetyl-Alpha-D-glucosaminidase deficiency",
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                            {
                                "id": "MONDO:0009656",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009656",
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                                "id": "MONDO:0009656",
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                            {
                                "id": "MONDO:0009656",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009656",
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                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/252920",
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                                "id": "0009656",
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                            {
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                                "id": "0111394",
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                    "germline",
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            },
            {
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                    "germline"
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                    {
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                            {
                                "id": "MONDO:0005575",
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                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
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                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
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                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
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                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
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                                "description": ""
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                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
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                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
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                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer with chromosomal instability, somatic",
                                "description": ""
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                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
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                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
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                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
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                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
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                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
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                            {
                                "id": "MONDO:0005575",
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                            {
                                "id": "MONDO:0005575",
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                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
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                            {
                                "id": "MONDO:0005575",
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                                "id": "MONDO:0005575",
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                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
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                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
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                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
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                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
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                                "id": "MONDO:0005575",
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                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
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                            {
                                "id": "MONDO:0005575",
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                                "id": "MONDO:0005575",
                                "resource": "MONDO",
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                                "id": "MONDO:0005575",
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                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
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                                "id": "MONDO:0005575",
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                                "id": "MONDO:0005575",
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                                "id": "MONDO:0014665",
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                                "url": "https://monarchinitiative.org/disease/MONDO:0009656",
                                "name": "mucopolysaccharidosis type IIIB (Sanfilippo B)",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009656",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009656",
                                "name": "MPS 3B",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009656",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009656",
                                "name": "MPS IIIB",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009656",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009656",
                                "name": "Mucopoly-saccharidosis type 3B",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009656",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009656",
                                "name": "N-Acetyl-Alpha-D-glucosaminidase deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009656",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009656",
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                                "description": ""
                            },
                            {
                                "id": "MONDO:0009656",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009656",
                                "name": "mucopolysaccharidosis, type 3B",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009656",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009656",
                                "name": "mucopolysaccharidosis, type IIIB",
                                "description": ""
                            },
                            {
                                "id": "MIM:252920",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/252920",
                                "name": "Mucopolysaccharidosis 3B",
                                "description": "Mucopolysaccharidosis 3B"
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                        ],
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                        "evidence": [
                            {
                                "id": "0009656",
                                "database": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009656"
                            },
                            {
                                "id": "252920",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/252920"
                            },
                            {
                                "id": "4669",
                                "database": "GlyCosmos",
                                "url": "https://glycosmos.org/glycogenes/show/4669#disease"
                            },
                            {
                                "id": "0111394",
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                        ]
                    },
                    {
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                            "id": "DOID:0111394",
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                            "url": "http://disease-ontology.org/term/DOID:0111394",
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                            {
                                "id": "DOID:0111394",
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                            {
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                                "resource": "Disease Ontology",
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                                "description": ""
                            },
                            {
                                "id": "DOID:0111394",
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                            {
                                "id": "DOID:0111394",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0111394",
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                            },
                            {
                                "id": "DOID:0111394",
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                                "url": "http://disease-ontology.org/term/DOID:0111394",
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                            },
                            {
                                "id": "DOID:0111394",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0111394",
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                            },
                            {
                                "id": "DOID:0111394",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0111394",
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                            },
                            {
                                "id": "DOID:0111394",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0111394",
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                            },
                            {
                                "id": "MONDO:0009656",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009656",
                                "name": "mucopolysaccharidosis type 3B",
                                "description": "A rare autosomal recessive lysosomal storage disease caused by deficiency of the enzyme N-acetyl-alpha-D-glucosaminidase. It is characterized by behavioral changes, sleep disturbances, and mental developmental delays."
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                            {
                                "id": "MONDO:0009656",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009656",
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                                "description": ""
                            },
                            {
                                "id": "MONDO:0009656",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009656",
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                                "description": ""
                            },
                            {
                                "id": "MONDO:0009656",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009656",
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                                "description": ""
                            },
                            {
                                "id": "MONDO:0009656",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009656",
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                            },
                            {
                                "id": "MONDO:0009656",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009656",
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                                "description": ""
                            },
                            {
                                "id": "MONDO:0009656",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009656",
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                                "description": ""
                            },
                            {
                                "id": "MONDO:0009656",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009656",
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                            {
                                "id": "MONDO:0009656",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009656",
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                            },
                            {
                                "id": "MONDO:0009656",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009656",
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                                "description": ""
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                            {
                                "id": "MONDO:0009656",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009656",
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                            {
                                "id": "MONDO:0009656",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009656",
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                                "description": ""
                            },
                            {
                                "id": "MONDO:0009656",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009656",
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                            {
                                "id": "MONDO:0009656",
                                "resource": "MONDO",
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                            {
                                "id": "MONDO:0009656",
                                "resource": "MONDO",
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                            {
                                "id": "MONDO:0009656",
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                            {
                                "id": "MONDO:0009656",
                                "resource": "MONDO",
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                            {
                                "id": "MONDO:0009656",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009656",
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            },
            {
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            },
            {
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                    "germline"
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            },
            {
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                ],
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                "keywords": [
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                    "germline"
                ]
            },
            {
                "evidence": [
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                    {
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                    {
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                "sequence_mut": "L",
                "comment": "Germline mutation passed 0 out of 0 filters:",
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            },
            {
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                    {
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                "glycoeffect": [],
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                "sequence_org": "F",
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                    "ebi",
                    "germline"
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            },
            {
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                    {
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                "sequence_org": "C",
                "sequence_mut": "W",
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                "chr_pos": "42536563",
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                            {
                                "id": "MONDO:0014665",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0014665",
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                            {
                                "id": "MONDO:0014665",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0014665",
                                "name": "Charcot-Marie-Tooth disease caused by mutation in NAGLU",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0014665",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0014665",
                                "name": "Charcot-Marie-Tooth neuropathy type 2V",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0014665",
                                "resource": "MONDO",
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                            },
                            {
                                "id": "MONDO:0014665",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0014665",
                                "name": "autosomal dominant Charcot-Marie-Tooth disease type 2 due to NAGLU mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0014665",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0014665",
                                "name": "autosomal dominant Charcot-Marie-Tooth disease type 2V",
                                "description": ""
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                            {
                                "id": "MONDO:0014665",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0014665",
                                "name": "autosomal dominant axonal Charcot-Marie-Tooth disease type 2V",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0014665",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0014665",
                                "name": "hereditary adult-onset painful axonal polyneuropathy",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0014665",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0014665",
                                "name": "Charcot-Marie-Tooth disease, axonal, autosomal dominant, type 2V",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0014665",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0014665",
                                "name": "Charcot-Marie-Tooth disease, axonal, type 2V",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0014665",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0014665",
                                "name": "Charcot-Marie-Tooth neuropathy, type 2V",
                                "description": ""
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                                "id": "616491",
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                            {
                                "id": "0110178",
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                        ]
                    },
                    {
                        "disease_id": "DOID:0110178",
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                                "id": "DOID:0110178",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0110178",
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                            {
                                "id": "DOID:0110178",
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                                "id": "DOID:0110178",
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                                "id": "DOID:0110178",
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                            {
                                "id": "MONDO:0014665",
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                            {
                                "id": "MONDO:0014665",
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                                "name": "Charcot-Marie-Tooth disease caused by mutation in NAGLU",
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                            {
                                "id": "MONDO:0014665",
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                                "description": ""
                            },
                            {
                                "id": "MONDO:0014665",
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                            {
                                "id": "MONDO:0014665",
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                                "id": "MONDO:0014665",
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                                "id": "MONDO:0009656",
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                            {
                                "id": "MONDO:0009656",
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                            {
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                            {
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                            {
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                "minor_allelic_frequency": "",
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                                "database": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009656"
                            },
                            {
                                "id": "252920",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/252920"
                            },
                            {
                                "id": "4669",
                                "database": "GlyCosmos",
                                "url": "https://glycosmos.org/glycogenes/show/4669#disease"
                            },
                            {
                                "id": "0111394",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0111394"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0111394",
                        "recommended_name": {
                            "id": "DOID:0111394",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:0111394",
                            "name": "mucopolysaccharidosis type IIIB",
                            "description": "A mucopolysaccharidosis III characterized by neurodegeneration, behavioral problems, mild skeletal changes, and shortened life span that has_material_basis_in homozygous or compound heterozygous mutation in NAGLU on chromosome 17q21.2."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0111394",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0111394",
                                "name": "MPS3B",
                                "description": ""
                            },
                            {
                                "id": "DOID:0111394",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0111394",
                                "name": "MPSIIIB",
                                "description": ""
                            },
                            {
                                "id": "DOID:0111394",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0111394",
                                "name": "Mucopoly-saccharidosis type 3B",
                                "description": ""
                            },
                            {
                                "id": "DOID:0111394",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0111394",
                                "name": "Mucopolysaccharidosis type 3B",
                                "description": ""
                            },
                            {
                                "id": "DOID:0111394",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0111394",
                                "name": "N-acetyl-alpha-glucosaminidase deficiency",
                                "description": ""
                            },
                            {
                                "id": "DOID:0111394",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0111394",
                                "name": "NAGLU deficiency",
                                "description": ""
                            },
                            {
                                "id": "DOID:0111394",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0111394",
                                "name": "Sanfilippo syndrome type B",
                                "description": ""
                            },
                            {
                                "id": "DOID:0111394",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0111394",
                                "name": "mucopolysaccharidosis type IIIB (Sanfilippo B)",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009656",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009656",
                                "name": "mucopolysaccharidosis type 3B",
                                "description": "A rare autosomal recessive lysosomal storage disease caused by deficiency of the enzyme N-acetyl-alpha-D-glucosaminidase. It is characterized by behavioral changes, sleep disturbances, and mental developmental delays."
                            },
                            {
                                "id": "MONDO:0009656",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009656",
                                "name": "MPS III B",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009656",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009656",
                                "name": "MPS3B",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009656",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009656",
                                "name": "MPSIIIB",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009656",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009656",
                                "name": "N-acetyl-alpha-glucosaminidase deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009656",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009656",
                                "name": "Sanfilippo B",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009656",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009656",
                                "name": "Sanfilippo syndrome B",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009656",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009656",
                                "name": "Sanfilippo syndrome type B",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009656",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009656",
                                "name": "mucopolysaccharidosis type 3B",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009656",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009656",
                                "name": "mucopolysaccharidosis type IIIB",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009656",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009656",
                                "name": "mucopolysaccharidosis type IIIB (Sanfilippo B)",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009656",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009656",
                                "name": "MPS 3B",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009656",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009656",
                                "name": "MPS IIIB",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009656",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009656",
                                "name": "Mucopoly-saccharidosis type 3B",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009656",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009656",
                                "name": "N-Acetyl-Alpha-D-glucosaminidase deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009656",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009656",
                                "name": "NAGLU deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009656",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009656",
                                "name": "mucopolysaccharidosis, type 3B",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009656",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009656",
                                "name": "mucopolysaccharidosis, type IIIB",
                                "description": ""
                            },
                            {
                                "id": "MIM:252920",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/252920",
                                "name": "Mucopolysaccharidosis 3B",
                                "description": "Mucopolysaccharidosis 3B"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0009656",
                                "database": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009656"
                            },
                            {
                                "id": "252920",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/252920"
                            },
                            {
                                "id": "4669",
                                "database": "GlyCosmos",
                                "url": "https://glycosmos.org/glycogenes/show/4669#disease"
                            },
                            {
                                "id": "0111394",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0111394"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ]
            }
        ]
    }
}
