{
    "disease_id": "DOID:0060248",
    "recommended_name": {
        "id": "DOID:0060248",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0060248",
        "name": "Simpson-Golabi-Behmel syndrome type 1",
        "description": "A syndrome characterized by pre- and postnatal overgrowth and craniofacial, skeletal, cardiac and renal abnormalities and has_material_basis_in mutation in the gene encoding glypican-3 on chromosome Xq26."
    },
    "synonyms": [
        {
            "id": "DOID:0060248",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060248",
            "name": "DGSX Golabi-Rosen syndrome",
            "description": ""
        },
        {
            "id": "DOID:0060248",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060248",
            "name": "Golabi-Rosen syndrome",
            "description": ""
        },
        {
            "id": "DOID:0060248",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060248",
            "name": "SGB syndrome",
            "description": ""
        },
        {
            "id": "DOID:0060248",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060248",
            "name": "Sara Angers syndrome",
            "description": ""
        },
        {
            "id": "DOID:0060248",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060248",
            "name": "Simpson dysmorphia syndrome",
            "description": ""
        },
        {
            "id": "DOID:0060248",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060248",
            "name": "X-linked dysplasia gigantism syndrome",
            "description": ""
        },
        {
            "id": "DOID:0060248",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060248",
            "name": "bulldog syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0020602",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0020602",
            "name": "Simpson-Golabi-Behmel syndrome type 1",
            "description": "Any Simpson-Golabi-Behmel syndrome in which the cause of the disease is a mutation in the GPC3 gene."
        },
        {
            "id": "MONDO:0020602",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0020602",
            "name": "dysplasia gigantism syndrome, X-linked",
            "description": ""
        },
        {
            "id": "MONDO:0020602",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0020602",
            "name": "GPC3 Simpson-Golabi-Behmel syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0020602",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0020602",
            "name": "Simpson-Golabi-Behmel syndrome caused by mutation in GPC3",
            "description": ""
        },
        {
            "id": "MONDO:0020602",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0020602",
            "name": "Simpson-Golabi-Behmel syndrome type 1",
            "description": ""
        },
        {
            "id": "MONDO:0020602",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0020602",
            "name": "Golabi-Rosen syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0020602",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0020602",
            "name": "Simpson-Golabi-Behmel syndrome, type 1; SGBS1",
            "description": ""
        },
        {
            "id": "MONDO:0020602",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0020602",
            "name": "Simpson dysmorphia syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0020602",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0020602",
            "name": "bulldog syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0020602",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0020602",
            "name": "Simpson-Golabi-Behmel syndrome, type 1",
            "description": ""
        },
        {
            "id": "MONDO:0020602",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0020602",
            "name": "Sgbs",
            "description": ""
        },
        {
            "id": "MONDO:0020602",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0020602",
            "name": "SGBS1",
            "description": ""
        },
        {
            "id": "MONDO:0020602",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0020602",
            "name": "DGSX Golabi-Rosen syndrome",
            "description": ""
        },
        {
            "id": "MIM:312870",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/312870",
            "name": "Simpson-Golabi-Behmel syndrome 1",
            "description": "Simpson-Golabi-Behmel syndrome 1"
        }
    ]
}