{
    "disease_id": "DOID:0111845", 
    "synonyms": [
        {
            "url": "http://disease-ontology.org/term/DOID:0111845", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111845", 
            "name": "NEDXCF"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111845", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111845", 
            "name": "MKMS"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111845", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111845", 
            "name": "X-linked neurodevelopmental disorder with craniofacial abnormalities"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111845", 
        "description": "A syndromic X-linked intellectual disability characterized by global developmental delay with impaired intellectual development and poor speech and commonly associated with ear abnormalities, hearing loss, and dysmorphic facial features that has_material_basis_in heterozygous or hemizygous mutation in STAG2 on chromosome Xq25.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111845", 
        "name": "Mullegama-Klein-Martinez syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111845#disease-associations", 
            "id": "0111845", 
            "database": "Alliance of Genome Resources"
        }
    ]
}