{
    "disease_id": "DOID:0112153",
    "recommended_name": {
        "id": "DOID:0112153",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0112153",
        "name": "hypomyelinating leukodystrophy 20",
        "description": "A hypomyelinating leukodystrophy characterized by progressive loss of developmental milestones starting at about 12 to 16 months of age after normal early development that has_material_basis_in homozygous or compound heterozygous mutation in CNP on chromosome 17q21.2."
    },
    "synonyms": [
        {
            "id": "DOID:0112153",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0112153",
            "name": "HLD20",
            "description": ""
        },
        {
            "id": "MIM:619071",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/619071",
            "name": "Leukodystrophy, hypomyelinating, 20",
            "description": "Leukodystrophy, hypomyelinating, 20"
        }
    ]
}