{
    "disease_id": "DOID:0111560",
    "recommended_name": {
        "id": "DOID:0111560",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0111560",
        "name": "Charcot-Marie-Tooth disease type 1G",
        "description": "A Charcot-Marie-Tooth disease type 1 characterized by distal muscle weakness and atrophy with onset in the first or second decade of life that has_material_basis_in heterozygous mutation in PMP2 on chromosome 8q21.13."
    },
    "synonyms": [
        {
            "id": "DOID:0111560",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111560",
            "name": "CMT1G",
            "description": ""
        },
        {
            "id": "DOID:0111560",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111560",
            "name": "PMP2-related hereditary motor and sensory neuropathy type 1",
            "description": ""
        },
        {
            "id": "DOID:0111560",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111560",
            "name": "PMP2-related CMT1",
            "description": ""
        },
        {
            "id": "DOID:0111560",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111560",
            "name": "PMP2-related Charcot-Marie-Tooth disease type 1",
            "description": ""
        },
        {
            "id": "DOID:0111560",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111560",
            "name": "PMP2-related Charcot-Marie-Tooth neuropathy type 1",
            "description": ""
        },
        {
            "id": "MIM:618279",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/618279",
            "name": "Charcot-Marie-Tooth disease, demyelinating, 1G",
            "description": "Charcot-Marie-Tooth disease, demyelinating, 1G"
        }
    ]
}