{
    "disease_id": "DOID:0060795", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014813", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014813", 
            "name": "HIKESHI leukodystrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014813", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014813", 
            "name": "HLD13"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014813", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014813", 
            "name": "hypomyelinating leukodystrophy type 13"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014813", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014813", 
            "name": "leukodystrophy, hypomyelinating, 13; HLD13"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014813", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014813", 
            "name": "leukodystrophy caused by mutation in HIKESHI"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014813", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014813", 
            "name": "leukodystrophy, hypomyelinating, 13"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014813", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014813", 
            "name": "leukodystrophy, hypomyelinating, type 13"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060795", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060795", 
            "name": "HLD13"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060795", 
        "description": "A hypomyelinating leukodystrophy characterized by autosomal recessive inheritance of infantile onset of delayed psychomotor development, axial hypotonia, and spasticity associated with delayed myelination and periventricular white matter abnormalities that has_material_basis_in homozygous mutation in the C11ORF73 gene on chromosome 11q14.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060795", 
        "name": "hypomyelinating leukodystrophy 13"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060795#disease-associations", 
            "id": "0060795", 
            "database": "Alliance of Genome Resources"
        }
    ]
}