{
    "disease_id": "DOID:0060791", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014506", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014506", 
            "name": "RARS-related autosomal recessive hypomyelinating leukodystrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014506", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014506", 
            "name": "leukodystrophy caused by mutation in RARS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014506", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014506", 
            "name": "RARS leukodystrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014506", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014506", 
            "name": "HLD9"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014506", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014506", 
            "name": "leukodystrophy, hypomyelinating, type 9"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014506", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014506", 
            "name": "leukodystrophy, hypomyelinating, 9; HLD9"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014506", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014506", 
            "name": "leukodystrophy, hypomyelinating, 9"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014506", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014506", 
            "name": "hypomyelinating leukodystrophy type 9"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060791", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060791", 
            "name": "HLD9"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060791", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060791", 
            "name": "RARS-related autosomal recessive hypomyelinating leukodystrophy"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060791", 
        "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.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060791", 
        "name": "hypomyelinating leukodystrophy 9"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060791#disease-associations", 
            "id": "0060791", 
            "database": "Alliance of Genome Resources"
        }
    ]
}