{
    "disease_id": "DOID:0080107", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014592", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014592", 
            "name": "microcephaly and chorioretinopathy type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014592", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014592", 
            "name": "microcephaly and chorioretinopathy, autosomal recessive, 3; MCCRP3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014592", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014592", 
            "name": "TUBGCP4 microcephaly and chorioretinopathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014592", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014592", 
            "name": "MCCRP3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014592", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014592", 
            "name": "microcephaly and chorioretinopathy, autosomal recessive, 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014592", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014592", 
            "name": "microcephaly and chorioretinopathy caused by mutation in TUBGCP4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014592", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014592", 
            "name": "microcephaly and chorioretinopathy, autosomal recessive, type 3"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080107", 
        "description": "A syndrome that is characterized by congenital microcephaly and chorioretinal dysplasia associated with poor vision and nystagmus and has_material_basis_in compound heterozygous mutation in the TUBGCP4 gene.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080107", 
        "name": "microcephaly and chorioretinopathy 3"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0080107#disease-associations", 
            "id": "0080107", 
            "database": "Alliance of Genome Resources"
        }
    ]
}