{
    "disease_id": "DOID:14711", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010590", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010590", 
            "name": "FG syndrome 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010590", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010590", 
            "name": "Opitz-Kaveggia syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010590", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010590", 
            "name": "FG syndrome type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010590", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010590", 
            "name": "Opitz-Kaveggia syndrome; OKS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010590", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010590", 
            "name": "MED12 FG syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010590", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010590", 
            "name": "Keller syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010590", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010590", 
            "name": "FG syndrome caused by mutation in MED12"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010590", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010590", 
            "name": "OKS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010590", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010590", 
            "name": "mental retardation, large head, imperforate anus, congenital hypotonia, and partial agenesis of corpus callosum"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:14711", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:14711", 
            "name": "Keller syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:14711", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:14711", 
            "name": "Opitz-Kaveggia syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:14711", 
        "description": "A syndrome characterized by retardation, hyperactivity, hypotonia, broad thumbs, big first toes and a characteristic facial appearance including macrocephaly and has an X-linked recessive inheritance pattern.", 
        "resource": "Disease Ontology", 
        "id": "DOID:14711", 
        "name": "FG syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/14711#disease-associations", 
            "id": "14711", 
            "database": "Alliance of Genome Resources"
        }
    ]
}