{
    "disease_id": "DOID:0070679",
    "recommended_name": {
        "id": "DOID:0070679",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0070679",
        "name": "congenital hypomyelinating neuropathy 2",
        "description": "A congenital hypomyelinating neuropathy that has_material_basis_in heterozygous mutation in the MPZ gene on chromosome 1q23."
    },
    "synonyms": [
        {
            "id": "DOID:0070679",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070679",
            "name": "CHN2",
            "description": ""
        },
        {
            "id": "MONDO:0020765",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0020765",
            "name": "neuropathy, congenital hypomyelinating, 2",
            "description": ""
        },
        {
            "id": "MONDO:0020765",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0020765",
            "name": "CHN2",
            "description": ""
        },
        {
            "id": "MONDO:0020765",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0020765",
            "name": "NEUROPATHY, CONGENITAL HYPOMYELINATING, 2",
            "description": ""
        },
        {
            "id": "MONDO:0020765",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0020765",
            "name": "hypomyelinating neuropathy, congenital, 2",
            "description": ""
        },
        {
            "id": "MIM:618184",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/618184",
            "name": "Neuropathy, congenital hypomyelinating, 2",
            "description": "Neuropathy, congenital hypomyelinating, 2"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0070679"
    ],
    "unlinked_id_list": []
}