{
    "disease_id": "DOID:0080226", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0030922", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0030922", 
            "name": "intellectual disability, autosomal dominant 56"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0030922", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0030922", 
            "name": "MRD56"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0030922", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0030922", 
            "name": "mental retardation, autosomal dominant 56"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0030922", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0030922", 
            "name": "mental retardation, autosomal dominant 56; MRD56"
        }, 
        {
            "url": "https://www.omim.org/entry/617854", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:617854", 
            "name": "Mental retardation, autosomal dominant 56"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080226", 
        "description": "A syndromic intellectual disability characterized by global developmental delay, intellectual disability and in most cases hypotonia, delayed walking, poor fine motor skills, and poor or absent speech that has_material_basis_in heterozygous mutation in the CLTC gene on chromosome 17q23.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080226", 
        "name": "autosomal dominant mental retardation 56"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/617854", 
            "id": "617854", 
            "database": "MIM"
        }
    ]
}