{
    "disease_id": "DOID:0080106", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014516", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014516", 
            "name": "microcephaly and chorioretinopathy caused by mutation in PLK4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014516", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014516", 
            "name": "microcephaly and chorioretinopathy, autosomal recessive, 2; MCCRP2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014516", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014516", 
            "name": "MCCRP2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014516", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014516", 
            "name": "microcephaly and chorioretinopathy, autosomal recessive, type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014516", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014516", 
            "name": "microcephaly and chorioretinopathy, autosomal recessive, 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014516", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014516", 
            "name": "microcephaly and chorioretinopathy type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014516", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014516", 
            "name": "PLK4 microcephaly and chorioretinopathy"
        }, 
        {
            "url": "https://www.omim.org/entry/616171", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:616171", 
            "name": "Microcephaly and chorioretinopathy, autosomal recessive, 2"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080106", 
        "description": "A syndrome that is characterized by delayed psychomotor development, visual impairment, and short stature and has_material_basis_in homozygous mutation in the PLK4 gene.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080106", 
        "name": "microcephaly and chorioretinopathy 2"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/616171", 
            "id": "616171", 
            "database": "MIM"
        }
    ]
}