{
    "disease_id": "DOID:0070405",
    "recommended_name": {
        "id": "DOID:0070405",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0070405",
        "name": "hypomyelinating leukodystrophy 16",
        "description": "A hypomyelinating leukodystrophy characterized by onset of hypotonia, nystagmus, and mildly delayed motor development in infancy that has_material_basis_in heterozygous mutation in the TMEM106B gene on chromosome 7p21."
    },
    "synonyms": [
        {
            "id": "DOID:0070405",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070405",
            "name": "HLD16",
            "description": ""
        },
        {
            "id": "MONDO:0054791",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0054791",
            "name": "leukodystrophy, hypomyelinating, 16",
            "description": ""
        },
        {
            "id": "MONDO:0054791",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0054791",
            "name": "leukodystrophy, hypomyelinating, 16",
            "description": ""
        },
        {
            "id": "MONDO:0054791",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0054791",
            "name": "HLD16",
            "description": ""
        },
        {
            "id": "MIM:617964",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/617964",
            "name": "Leukodystrophy, hypomyelinating, 16",
            "description": "Leukodystrophy, hypomyelinating, 16"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0070405"
    ],
    "unlinked_id_list": []
}