{
    "disease_id": "DOID:0060791",
    "recommended_name": {
        "id": "DOID:0060791",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0060791",
        "name": "hypomyelinating leukodystrophy 9",
        "description": "A hypomyelinating leukodystrophy characterized by delayed psychomotor development, spasticity, and nystagmus starting in the first year of life that has_material_basis_in compound heterozygous mutation in the RARS gene on chromosome 5q34."
    },
    "synonyms": [
        {
            "id": "DOID:0060791",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060791",
            "name": "HLD9",
            "description": ""
        },
        {
            "id": "DOID:0060791",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060791",
            "name": "RARS-related autosomal recessive hypomyelinating leukodystrophy",
            "description": ""
        },
        {
            "id": "MONDO:0014506",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014506",
            "name": "hypomyelinating leukodystrophy 9",
            "description": "Any leukodystrophy in which the cause of the disease is a mutation in the RARS gene."
        },
        {
            "id": "MONDO:0014506",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014506",
            "name": "HLD9",
            "description": ""
        },
        {
            "id": "MONDO:0014506",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014506",
            "name": "RARS leukodystrophy",
            "description": ""
        },
        {
            "id": "MONDO:0014506",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014506",
            "name": "RARS-related autosomal recessive hypomyelinating leukodystrophy",
            "description": ""
        },
        {
            "id": "MONDO:0014506",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014506",
            "name": "hypomyelinating leukodystrophy type 9",
            "description": ""
        },
        {
            "id": "MONDO:0014506",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014506",
            "name": "leukodystrophy caused by mutation in RARS",
            "description": ""
        },
        {
            "id": "MONDO:0014506",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014506",
            "name": "leukodystrophy, hypomyelinating, type 9",
            "description": ""
        },
        {
            "id": "MONDO:0014506",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014506",
            "name": "leukodystrophy, hypomyelinating, 9",
            "description": ""
        },
        {
            "id": "MIM:616140",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/616140",
            "name": "Leukodystrophy, hypomyelinating, 9",
            "description": "Leukodystrophy, hypomyelinating, 9"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0060791"
    ],
    "unlinked_id_list": []
}