{
    "disease_id": "DOID:0110152",
    "recommended_name": {
        "id": "DOID:0110152",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0110152",
        "name": "Charcot-Marie-Tooth disease type 1B",
        "description": "A Charcot-Marie-Tooth disease type 1 that has_material_basis_in heterozygous mutation in the gene encoding myelin protein zero (MPZ)."
    },
    "synonyms": [
        {
            "id": "DOID:0110152",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110152",
            "name": "CMT1B",
            "description": ""
        },
        {
            "id": "DOID:0110152",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110152",
            "name": "Charcot-Marie-Tooth neuropathy type 1B",
            "description": ""
        },
        {
            "id": "DOID:0110152",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110152",
            "name": "Charcot-Marie-Tooth disease slow nerve conduction type linked to Duffy",
            "description": ""
        },
        {
            "id": "DOID:0110152",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110152",
            "name": "HMSN IB",
            "description": ""
        },
        {
            "id": "DOID:0110152",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110152",
            "name": "HMSN1B",
            "description": ""
        },
        {
            "id": "DOID:0110152",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110152",
            "name": "autosomal dominant Charcot-Marie-Tooth disease with focally folded myelin sheaths type 1B",
            "description": ""
        },
        {
            "id": "DOID:0110152",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110152",
            "name": "hereditary motor and sensory neuropathy IB",
            "description": ""
        },
        {
            "id": "DOID:0110152",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110152",
            "name": "peroneal muscular atrophy",
            "description": ""
        },
        {
            "id": "MONDO:0007307",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007307",
            "name": "Charcot-Marie-Tooth disease type 1B",
            "description": "A sensorineural peripheral polyneuropathy affecting approximately 1 in 2,500 individuals, and is the most common inherited disorder of the peripheral nervous system. Autosomal dominant, autosomal recessive, and X-linked forms have been recognized."
        },
        {
            "id": "MONDO:0007307",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007307",
            "name": "CMT1B",
            "description": ""
        },
        {
            "id": "MONDO:0007307",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007307",
            "name": "Charcot-Marie-Tooth disease slow nerve conduction type linked to Duffy",
            "description": ""
        },
        {
            "id": "MONDO:0007307",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007307",
            "name": "Charcot-Marie-Tooth disease type 1 caused by mutation in MPZ",
            "description": ""
        },
        {
            "id": "MONDO:0007307",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007307",
            "name": "Charcot-Marie-Tooth disease, type 1B",
            "description": ""
        },
        {
            "id": "MONDO:0007307",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007307",
            "name": "Charcot-Marie-Tooth neuropathy type 1B",
            "description": ""
        },
        {
            "id": "MONDO:0007307",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007307",
            "name": "HMSN IB",
            "description": ""
        },
        {
            "id": "MONDO:0007307",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007307",
            "name": "HMSN1B",
            "description": ""
        },
        {
            "id": "MONDO:0007307",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007307",
            "name": "MPZ Charcot-Marie-Tooth disease type 1",
            "description": ""
        },
        {
            "id": "MONDO:0007307",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007307",
            "name": "autosomal dominant Charcot-Marie-Tooth disease with focally folded myelin sheaths type 1B",
            "description": ""
        },
        {
            "id": "MONDO:0007307",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007307",
            "name": "hereditary motor and sensory neuropathy IB",
            "description": ""
        },
        {
            "id": "MONDO:0007307",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007307",
            "name": "CMT 1B",
            "description": ""
        },
        {
            "id": "MONDO:0007307",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007307",
            "name": "Charcot Marie Tooth disease type 1B",
            "description": ""
        },
        {
            "id": "MONDO:0007307",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007307",
            "name": "Charcot-Marie-Tooth disease, autosomal dominant, with focally folded myelin sheaths, type 1B",
            "description": ""
        },
        {
            "id": "MONDO:0007307",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007307",
            "name": "Charcot-Marie-Tooth disease, demyelinating, type 1B",
            "description": ""
        },
        {
            "id": "MONDO:0007307",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007307",
            "name": "Charcot-Marie-Tooth disease, slow nerve conduction type, linked to Duffy",
            "description": ""
        },
        {
            "id": "MONDO:0007307",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007307",
            "name": "Charcot-Marie-Tooth neuropathy, type 1B",
            "description": ""
        },
        {
            "id": "MONDO:0007307",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007307",
            "name": "HMSN 1B",
            "description": ""
        },
        {
            "id": "MONDO:0007307",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007307",
            "name": "HMSN1",
            "description": ""
        },
        {
            "id": "MONDO:0007307",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007307",
            "name": "hereditary motor and sensory neuropathy 1",
            "description": ""
        },
        {
            "id": "MONDO:0007307",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007307",
            "name": "hereditary motor and sensory neuropathy 1B",
            "description": ""
        },
        {
            "id": "MIM:118200",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/118200",
            "name": "Charcot-Marie-Tooth disease, demyelinating, 1B",
            "description": "Charcot-Marie-Tooth disease, demyelinating, 1B"
        }
    ]
}