{
    "disease_id": "DOID:0060248", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0020602", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0020602", 
            "name": "dysplasia gigantism syndrome, X-linked"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0020602", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0020602", 
            "name": "GPC3 Simpson-Golabi-Behmel syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0020602", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0020602", 
            "name": "Simpson-Golabi-Behmel syndrome caused by mutation in GPC3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0020602", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0020602", 
            "name": "Golabi-Rosen syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0020602", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0020602", 
            "name": "Simpson-Golabi-Behmel syndrome, type 1; SGBS1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0020602", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0020602", 
            "name": "Simpson dysmorphia syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0020602", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0020602", 
            "name": "bulldog syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0020602", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0020602", 
            "name": "Simpson-Golabi-Behmel syndrome, type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0020602", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0020602", 
            "name": "Sgbs"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0020602", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0020602", 
            "name": "SGBS1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0020602", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0020602", 
            "name": "DGSX Golabi-Rosen syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060248", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060248", 
            "name": "DGSX Golabi-Rosen syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060248", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060248", 
            "name": "Golabi-Rosen syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060248", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060248", 
            "name": "SGB syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060248", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060248", 
            "name": "Sara Angers syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060248", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060248", 
            "name": "Simpson dysmorphia syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060248", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060248", 
            "name": "X-linked dysplasia gigantism syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060248", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060248", 
            "name": "bulldog syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060248", 
        "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.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060248", 
        "name": "Simpson-Golabi-Behmel syndrome type 1"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060248#disease-associations", 
            "id": "0060248", 
            "database": "Alliance of Genome Resources"
        }
    ]
}