{
    "disease_id": "DOID:0070054", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014357", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014357", 
            "name": "intellectual disability, autosomal dominant 24"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014357", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014357", 
            "name": "mental retardation, autosomal dominant type 24"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014357", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014357", 
            "name": "autosomal dominant non-syndromic intellectual disability caused by mutation in DEAF1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014357", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014357", 
            "name": "autosomal dominant non-syndromic intellectual disability 24"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014357", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014357", 
            "name": "DEAF1 autosomal dominant non-syndromic intellectual disability"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014357", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014357", 
            "name": "mental retardation, autosomal dominant 24; MRD24"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014357", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014357", 
            "name": "MRD24"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014357", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014357", 
            "name": "mental retardation, autosomal dominant 24"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014357", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014357", 
            "name": "autosomal dominant mental retardation 24"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070054", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070054", 
            "name": "autosomal dominant non-syndromic intellectual disability 24"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070054", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070054", 
            "name": "MRD24"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070054", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070054", 
            "name": "autosomal dominant mental retardation 24"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070054", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070054", 
            "name": "IDDISBAS"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070054", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070054", 
            "name": "VSVS"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070054", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070054", 
            "name": "intellectual developmental disorder with impaired expressive speech and behavioral abnormalities, with or without seizures"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0070054", 
        "description": "An autosomal dominant non-syndromic intellectual disability characterized by delayed psychomotor development, poor expressive speech, and behavioral abnormalities that has_material_basis_in an autosomal dominant mutation of DEAF1 on chromosome 11p15.5.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0070054", 
        "name": "Vulto-van Silfout-de Vries syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/615828", 
            "id": "615828", 
            "database": "MIM"
        }
    ]
}