{
    "disease_id": "DOID:0111403", 
    "synonyms": [
        {
            "url": "http://disease-ontology.org/term/DOID:0111403", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111403", 
            "name": "MCCCHCM"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111403", 
        "description": "A syndromic intellectual disability characterized by global developmental delay, impaired intellectual development, and characteristic brain abnormalities that has_material_basis_in heterozygous mutation in MAST1 on chromosome 19p13.13.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111403", 
        "name": "mega-corpus-callosum syndrome with cerebellar hypoplasia and cortical malformations"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/618273", 
            "id": "618273", 
            "database": "MIM"
        }
    ]
}