{
    "disease_id": "DOID:0111674", 
    "synonyms": [
        {
            "url": "http://disease-ontology.org/term/DOID:0111674", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111674", 
            "name": "IDDSSBA"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111674", 
        "description": "A syndrome characterized by intellectual disability, global developmental delay, short stature, aphasia, and hypotonia that has_material_basis_in homozygous or compound heterozygous mutation in IQSEC1 on chromosome 3p25.2-p25.1.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111674", 
        "name": "intellectual developmental disorder with short stature and behavioral abnormalities"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111674#disease-associations", 
            "id": "0111674", 
            "database": "Alliance of Genome Resources"
        }
    ]
}