{
    "disease_id": "DOID:0060278", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014351", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014351", 
            "name": "pontocerebellar hypoplasia, type 9"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014351", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014351", 
            "name": "pontocerebellar hypoplasia, type 9; PCH9"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014351", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014351", 
            "name": "non-syndromic pontocerebellar hypoplasia caused by mutation in AMPD2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014351", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014351", 
            "name": "AMPD2 non-syndromic pontocerebellar hypoplasia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014351", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014351", 
            "name": "PCH9"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060278", 
        "description": "A pontocerebellar hypoplasia that is characterized by progressive microcephaly, spasticity, seizure and brain atrophy, has_material_basis_in autosomal recessive inheritance of mutation in the AMPD2 gene.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060278", 
        "name": "pontocerebellar hypoplasia type 9"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060278#disease-associations", 
            "id": "0060278", 
            "database": "Alliance of Genome Resources"
        }
    ]
}