{
    "disease_id": "DOID:0070400",
    "recommended_name": {
        "id": "DOID:0070400",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0070400",
        "name": "hypomyelinating leukodystrophy 19",
        "description": "A hypomyelinating leukodystrophy characterized by onset of transient neurologic abnormalities in early infancy with resolution within the first or second decades that has_material_basis_in heterozygous mutation in the TMEM63A gene on chromosome 1q42."
    },
    "synonyms": [
        {
            "id": "DOID:0070400",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070400",
            "name": "HLD19",
            "description": ""
        },
        {
            "id": "MONDO:0032871",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0032871",
            "name": "leukodystrophy, hypomyelinating, 19, transient infantile",
            "description": ""
        },
        {
            "id": "MONDO:0032871",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0032871",
            "name": "HLD19",
            "description": ""
        },
        {
            "id": "MIM:618688",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/618688",
            "name": "Leukodystrophy, hypomyelinating, 19, transient infantile",
            "description": "Leukodystrophy, hypomyelinating, 19, transient infantile"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0070400"
    ],
    "unlinked_id_list": []
}