{
    "disease_id": "DOID:0070285", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009617", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009617", 
            "name": "microcephaly 1, primary, autosomal recessive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009617", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009617", 
            "name": "premature chromosome condensation with microcephaly and mental retardation"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009617", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009617", 
            "name": "autosomal recessive primary microcephaly caused by mutation in MCPH1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009617", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009617", 
            "name": "MCPH1 autosomal recessive primary microcephaly"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009617", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009617", 
            "name": "premature chromosome condensation syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009617", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009617", 
            "name": "PCC syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009617", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009617", 
            "name": "microcephaly 1, primary, autosomal recessive; MCPH1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009617", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009617", 
            "name": "MCPH1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070285", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070285", 
            "name": "MCPH1"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0070285", 
        "description": "A primary autosomal recessive microcephaly that has_material_basis_in homozygous or compound heterozygous mutation in the MCPH1 gene on chromosome 8p23.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0070285", 
        "name": "primary autosomal recessive microcephaly 1"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0070285#disease-associations", 
            "id": "0070285", 
            "database": "Alliance of Genome Resources"
        }
    ]
}