{
    "disease_id": "DOID:0080107",
    "recommended_name": {
        "id": "DOID:0080107",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0080107",
        "name": "microcephaly and chorioretinopathy 3",
        "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."
    },
    "synonyms": [
        {
            "id": "MONDO:0014592",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014592",
            "name": "microcephaly and chorioretinopathy 3",
            "description": "Any microcephaly and chorioretinopathy in which the cause of the disease is a mutation in the TUBGCP4 gene."
        },
        {
            "id": "MONDO:0014592",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014592",
            "name": "microcephaly and chorioretinopathy type 3",
            "description": ""
        },
        {
            "id": "MONDO:0014592",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014592",
            "name": "microcephaly and chorioretinopathy, autosomal recessive, 3; MCCRP3",
            "description": ""
        },
        {
            "id": "MONDO:0014592",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014592",
            "name": "TUBGCP4 microcephaly and chorioretinopathy",
            "description": ""
        },
        {
            "id": "MONDO:0014592",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014592",
            "name": "MCCRP3",
            "description": ""
        },
        {
            "id": "MONDO:0014592",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014592",
            "name": "microcephaly and chorioretinopathy, autosomal recessive, 3",
            "description": ""
        },
        {
            "id": "MONDO:0014592",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014592",
            "name": "microcephaly and chorioretinopathy caused by mutation in TUBGCP4",
            "description": ""
        },
        {
            "id": "MONDO:0014592",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014592",
            "name": "microcephaly and chorioretinopathy, autosomal recessive, type 3",
            "description": ""
        },
        {
            "id": "MIM:616335",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/616335",
            "name": "Microcephaly and chorioretinopathy, autosomal recessive, 3",
            "description": "Microcephaly and chorioretinopathy, autosomal recessive, 3"
        }
    ]
}