{
    "disease_id": "DOID:0060788", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014632", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014632", 
            "name": "hypomyelinating leukodystrophy type 10"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014632", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014632", 
            "name": "leukodystrophy, hypomyelinating, type 10"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014632", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014632", 
            "name": "HLD10"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014632", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014632", 
            "name": "leukodystrophy, hypomyelinating, 10; HLD10"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014632", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014632", 
            "name": "leukodystrophy caused by mutation in PYCR2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014632", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014632", 
            "name": "leukodystrophy, hypomyelinating, 10"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014632", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014632", 
            "name": "PYCR2 leukodystrophy"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060788", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060788", 
            "name": "HLD10"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060788", 
        "description": "A hypomyelinating leukodystrophy characterized by autosomal recessive inheritance of progressive postnatal microcephaly, severely delayed psychomotor development and hypomyelination that has_material_basis_in homozygous mutation in the PYCR2 gene on chromosome 1q42.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060788", 
        "name": "hypomyelinating leukodystrophy 10"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060788#disease-associations", 
            "id": "0060788", 
            "database": "Alliance of Genome Resources"
        }
    ]
}