{
    "disease_id": "DOID:0060265", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011866", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011866", 
            "name": "pontocerebellar hypoplasia, type 1A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011866", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011866", 
            "name": "non-syndromic pontocerebellar hypoplasia caused by mutation in VRK1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011866", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011866", 
            "name": "pontocerebellar hypoplasia with infantile spinal muscular atrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011866", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011866", 
            "name": "pontocerebellar hypoplasia, type 1A; PCH1A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011866", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011866", 
            "name": "pontocerebellar hypoplasia with anterior horn cell disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011866", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011866", 
            "name": "PCH1A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011866", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011866", 
            "name": "VRK1 non-syndromic pontocerebellar hypoplasia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011866", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011866", 
            "name": "Pch1"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060265", 
        "description": "A pontocerebellar hypoplasia that is characterized by central and peripheral motor dysfunction, hypotonia, spasticity and failure to thrive, has_material_basis_in mutation in the VRK1 gene.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060265", 
        "name": "pontocerebellar hypoplasia type 1A"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060265#disease-associations", 
            "id": "0060265", 
            "database": "Alliance of Genome Resources"
        }
    ]
}