{
    "disease_id": "DOID:14711",
    "recommended_name": {
        "id": "DOID:14711",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:14711",
        "name": "FG syndrome",
        "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."
    },
    "synonyms": [
        {
            "id": "DOID:14711",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:14711",
            "name": "Keller syndrome",
            "description": ""
        },
        {
            "id": "DOID:14711",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:14711",
            "name": "Opitz-Kaveggia syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010366",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010366",
            "name": "FG syndrome 5",
            "description": ""
        },
        {
            "id": "MONDO:0010366",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010366",
            "name": "FGS5",
            "description": ""
        },
        {
            "id": "MONDO:0010366",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010366",
            "name": "FG syndrome 5; FGS5",
            "description": ""
        },
        {
            "id": "MONDO:0010366",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010366",
            "name": "FG syndrome 5",
            "description": ""
        },
        {
            "id": "MONDO:0010318",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010318",
            "name": "FG syndrome 4",
            "description": "Any FG syndrome in which the cause of the disease is a mutation in the CASK gene."
        },
        {
            "id": "MONDO:0010318",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010318",
            "name": "CASK FG syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010318",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010318",
            "name": "cask FG syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010318",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010318",
            "name": "mental retardation, X-linked, with or without Nystagmus",
            "description": ""
        },
        {
            "id": "MONDO:0010318",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010318",
            "name": "X-linked intellectual disability with or without nystagmus",
            "description": ""
        },
        {
            "id": "MONDO:0010318",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010318",
            "name": "FG syndrome 4",
            "description": ""
        },
        {
            "id": "MONDO:0010318",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010318",
            "name": "FG syndrome 4; FGS4",
            "description": ""
        },
        {
            "id": "MONDO:0010318",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010318",
            "name": "FG syndrome caused by mutation in CASK",
            "description": ""
        },
        {
            "id": "MONDO:0010318",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010318",
            "name": "FG syndrome caused by mutation in cask",
            "description": ""
        },
        {
            "id": "MONDO:0010318",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010318",
            "name": "FG syndrome type 4",
            "description": ""
        },
        {
            "id": "MONDO:0010318",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010318",
            "name": "FGS4",
            "description": ""
        },
        {
            "id": "MONDO:0010297",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010297",
            "name": "FG syndrome 2",
            "description": "Any FG syndrome in which the cause of the disease is a mutation in the FLNA gene."
        },
        {
            "id": "MONDO:0010297",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010297",
            "name": "FG syndrome caused by mutation in FLNA",
            "description": ""
        },
        {
            "id": "MONDO:0010297",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010297",
            "name": "FG syndrome 2; FGS2",
            "description": ""
        },
        {
            "id": "MONDO:0010297",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010297",
            "name": "FG syndrome type 2",
            "description": ""
        },
        {
            "id": "MONDO:0010297",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010297",
            "name": "FGS2",
            "description": ""
        },
        {
            "id": "MONDO:0010297",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010297",
            "name": "FG syndrome 2",
            "description": ""
        },
        {
            "id": "MONDO:0010297",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010297",
            "name": "FLNA FG syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010316",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010316",
            "name": "FG syndrome 3",
            "description": ""
        },
        {
            "id": "MONDO:0010316",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010316",
            "name": "FGS3",
            "description": ""
        },
        {
            "id": "MONDO:0010316",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010316",
            "name": "FG syndrome 3",
            "description": ""
        },
        {
            "id": "MONDO:0010316",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010316",
            "name": "FG syndrome 3; FGS3",
            "description": ""
        },
        {
            "id": "MONDO:0010590",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010590",
            "name": "FG syndrome 1",
            "description": "Any FG syndrome in which the cause of the disease is a mutation in the MED12 gene."
        },
        {
            "id": "MONDO:0010590",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010590",
            "name": "FG syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010590",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010590",
            "name": "Opitz-Kaveggia syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010590",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010590",
            "name": "FG syndrome type 1",
            "description": ""
        },
        {
            "id": "MONDO:0010590",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010590",
            "name": "Opitz-Kaveggia syndrome; OKS",
            "description": ""
        },
        {
            "id": "MONDO:0010590",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010590",
            "name": "MED12 FG syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010590",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010590",
            "name": "Keller syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010590",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010590",
            "name": "FG syndrome caused by mutation in MED12",
            "description": ""
        },
        {
            "id": "MONDO:0010590",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010590",
            "name": "FG syndrome 1",
            "description": ""
        },
        {
            "id": "MONDO:0010590",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010590",
            "name": "OKS",
            "description": ""
        },
        {
            "id": "MONDO:0010590",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010590",
            "name": "mental retardation, large head, imperforate anus, congenital hypotonia, and partial agenesis of corpus callosum",
            "description": ""
        },
        {
            "id": "MIM:300422",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/300422",
            "name": "FG syndrome 4",
            "description": "FG syndrome 4"
        },
        {
            "id": "MIM:300321",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/300321",
            "name": "FG syndrome 2",
            "description": "FG syndrome 2"
        },
        {
            "id": "MIM:305450",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/305450",
            "name": "Opitz-Kaveggia syndrome",
            "description": "Opitz-Kaveggia syndrome"
        }
    ]
}