{
    "disease_id": "DOID:0111838", 
    "synonyms": [
        {
            "url": "http://disease-ontology.org/term/DOID:0111838", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111838", 
            "name": "MRXS36"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111838", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111838", 
            "name": "X-linked syndromic mental retardation 36"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111838", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111838", 
            "name": "X-linked syndromic mental retardation Basilicata-Akhtar type"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111838", 
        "description": "A syndromic X-linked intellectual disability characterized by global developmental delay apparent from infancy, feeding difficulties, hypotonia, and poor or absent speech that has_material_basis_in hemizygous or heterozygous mutation in MSL3 on chromosome Xp22.2.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111838", 
        "name": "Basilicata-Akhtar syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111838#disease-associations", 
            "id": "0111838", 
            "database": "Alliance of Genome Resources"
        }
    ]
}