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                {
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            "subtype": {
                "name": "Biantennary"
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        },
        {
            "type": {
                "name": "N-linked",
                "url": ""
            },
            "subtype": {
                "name": "Complex",
                "url": ""
            }
        }
    ],
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        {
            "name": "6-Deoxy-Hexose",
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            "count": 0,
            "cid": "840",
            "url": "https://pubchem.ncbi.nlm.nih.gov/compound/840"
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        {
            "name": "Hexose",
            "residue": "hex",
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            "cid": "206",
            "url": "https://pubchem.ncbi.nlm.nih.gov/compound/206"
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        {
            "name": "N-Acetylhexosamine",
            "residue": "hexnac",
            "count": 4,
            "cid": "899",
            "url": "https://pubchem.ncbi.nlm.nih.gov/compound/899"
        },
        {
            "name": "Hexuronic Acid",
            "residue": "hexa",
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            "cid": "610",
            "url": "https://pubchem.ncbi.nlm.nih.gov/compound/610"
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        {
            "name": "2-Amino-2-Deoxy-Hexose",
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        {
            "name": "N-Acetyl-Neuraminic Acid",
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            "url": "https://pubchem.ncbi.nlm.nih.gov/compound/439197"
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        {
            "name": "N-Glycolyl-Neuraminic Acid",
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            "url": "https://pubchem.ncbi.nlm.nih.gov/compound/440001"
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        {
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            "url": "https://pubchem.ncbi.nlm.nih.gov/compound/1117"
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        {
            "id": "GGM.000001",
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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": "rs770171865",
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                        {
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                    ],
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                            "disease_id": "DOID:0111330",
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                            "evidence": [
                                {
                                    "id": "0111330",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111330"
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                            ]
                        },
                        {
                            "disease_id": "DOID:0111330",
                            "name": "combined saposin deficiency",
                            "description": "A sphingolipidosis characterized by absence of expression of both isoforms of PSAP (SAP1 and SAP2) resulting in hepatosplenomegaly and severe neurological disease that has_material_basis_in homozygous or compound heterozygous mutation in PSAP on 10q22.1.",
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                            "evidence": [
                                {
                                    "id": "0111330",
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                                    "url": "https://www.alliancegenome.org/disease/DOID:0111330"
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                            ]
                        },
                        {
                            "disease_id": "DOID:0111330",
                            "name": "combined saposin deficiency",
                            "description": "A sphingolipidosis characterized by absence of expression of both isoforms of PSAP (SAP1 and SAP2) resulting in hepatosplenomegaly and severe neurological disease that has_material_basis_in homozygous or compound heterozygous mutation in PSAP on 10q22.1.",
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                            "evidence": [
                                {
                                    "id": "0111330",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111330"
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                            ]
                        },
                        {
                            "disease_id": "DOID:0110961",
                            "name": "atypical Gaucher's disease due to saposin c deficiency",
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                            "evidence": [
                                {
                                    "id": "0110961",
                                    "database": "AGR",
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                                },
                                {
                                    "id": "0110961",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110961"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0110961",
                            "name": "atypical Gaucher's disease due to saposin c deficiency",
                            "description": "A Gaucher's disease that has_material_basis_in compound heterozygous mutation in the PSAP gene on chromosome 10q22.1.",
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                            "evidence": [
                                {
                                    "id": "0110961",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110961"
                                },
                                {
                                    "id": "0110961",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110961"
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                            "name": "metachromatic leukodystrophy",
                            "description": "A sphingolipidosis characterized by the accumulation of sulfatides in cells, especially the myelin producing cells of the nervous system.",
                            "url": "http://disease-ontology.org/term/DOID:10581",
                            "evidence": [
                                {
                                    "id": "10581",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:10581"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:10581",
                            "name": "metachromatic leukodystrophy",
                            "description": "A sphingolipidosis characterized by the accumulation of sulfatides in cells, especially the myelin producing cells of the nervous system.",
                            "url": "http://disease-ontology.org/term/DOID:10581",
                            "evidence": [
                                {
                                    "id": "10581",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:10581"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:10581",
                            "name": "metachromatic leukodystrophy",
                            "description": "A sphingolipidosis characterized by the accumulation of sulfatides in cells, especially the myelin producing cells of the nervous system.",
                            "url": "http://disease-ontology.org/term/DOID:10581",
                            "evidence": [
                                {
                                    "id": "10581",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:10581"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:10581",
                            "name": "metachromatic leukodystrophy",
                            "description": "A sphingolipidosis characterized by the accumulation of sulfatides in cells, especially the myelin producing cells of the nervous system.",
                            "url": "http://disease-ontology.org/term/DOID:10581",
                            "evidence": [
                                {
                                    "id": "10581",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:10581"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:10581",
                            "name": "metachromatic leukodystrophy",
                            "description": "A sphingolipidosis characterized by the accumulation of sulfatides in cells, especially the myelin producing cells of the nervous system.",
                            "url": "http://disease-ontology.org/term/DOID:10581",
                            "evidence": [
                                {
                                    "id": "10581",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:10581"
                                }
                            ]
                        }
                    ]
                }
            ],
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P07602-1",
                    "start_pos": 215,
                    "end_pos": 215,
                    "residue": "asn",
                    "evidence": [
                        {
                            "database": "PubMed",
                            "id": "11180632",
                            "url": "https://glygen.org/publication/PubMed/11180632"
                        },
                        {
                            "database": "UniCarbKB",
                            "id": "GLY_000040",
                            "url": "http://data.glygen.org/GLY_000040"
                        },
                        {
                            "database": "PubMed",
                            "id": "2110822",
                            "url": "https://glygen.org/publication/PubMed/2110822"
                        },
                        {
                            "database": "PubMed",
                            "id": "8344278",
                            "url": "https://glygen.org/publication/PubMed/8344278"
                        }
                    ],
                    "protein_name": "Prosaposin",
                    "gene_name": "PSAP",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
                    "length": 524,
                    "chemical_mass": 58113.0
                }
            ]
        }
    ],
    "record_id": "G00986YT"
}
