{
    "disease_id": "DOID:0070403",
    "recommended_name": {
        "id": "DOID:0070403",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0070403",
        "name": "hypomyelinating leukodystrophy 26",
        "description": "A hypomyelinating leukodystrophy characterized by severe psychomotor delay, predominantly involving motor and expressive language development, cerebral and cerebellar atrophy, and corpus callosum hypoplasia that has_material_basis_in homozygous mutation in the SLC35B2 gene on chromosome 6p21."
    },
    "synonyms": [
        {
            "id": "DOID:0070403",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070403",
            "name": "HLD26",
            "description": ""
        },
        {
            "id": "MONDO:0859518",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0859518",
            "name": "leukodystrophy, hypomyelinating, 26, with chondrodysplasia",
            "description": ""
        },
        {
            "id": "MIM:620269",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/620269",
            "name": "Leukodystrophy, hypomyelinating, 26, with chondrodysplasia",
            "description": "Leukodystrophy, hypomyelinating, 26, with chondrodysplasia"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0070403"
    ],
    "unlinked_id_list": []
}