{
    "disease_id": "DOID:0070054",
    "recommended_name": {
        "id": "DOID:0070054",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0070054",
        "name": "Vulto-van Silfout-de Vries syndrome",
        "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."
    },
    "synonyms": [
        {
            "id": "DOID:0070054",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070054",
            "name": "autosomal dominant non-syndromic intellectual disability 24",
            "description": ""
        },
        {
            "id": "DOID:0070054",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070054",
            "name": "MRD24",
            "description": ""
        },
        {
            "id": "DOID:0070054",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070054",
            "name": "autosomal dominant mental retardation 24",
            "description": ""
        },
        {
            "id": "DOID:0070054",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070054",
            "name": "IDDISBAS",
            "description": ""
        },
        {
            "id": "DOID:0070054",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070054",
            "name": "VSVS",
            "description": ""
        },
        {
            "id": "DOID:0070054",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070054",
            "name": "intellectual developmental disorder with impaired expressive speech and behavioral abnormalities, with or without seizures",
            "description": ""
        },
        {
            "id": "MONDO:0014357",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014357",
            "name": "intellectual disability, autosomal dominant 24",
            "description": "Any autosomal dominant non-syndromic intellectual disability in which the cause of the disease is a mutation in the DEAF1 gene."
        },
        {
            "id": "MONDO:0014357",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014357",
            "name": "mental retardation, autosomal dominant type 24",
            "description": ""
        },
        {
            "id": "MONDO:0014357",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014357",
            "name": "autosomal dominant non-syndromic intellectual disability caused by mutation in DEAF1",
            "description": ""
        },
        {
            "id": "MONDO:0014357",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014357",
            "name": "autosomal dominant non-syndromic intellectual disability 24",
            "description": ""
        },
        {
            "id": "MONDO:0014357",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014357",
            "name": "DEAF1 autosomal dominant non-syndromic intellectual disability",
            "description": ""
        },
        {
            "id": "MONDO:0014357",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014357",
            "name": "mental retardation, autosomal dominant 24; MRD24",
            "description": ""
        },
        {
            "id": "MONDO:0014357",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014357",
            "name": "MRD24",
            "description": ""
        },
        {
            "id": "MONDO:0014357",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014357",
            "name": "mental retardation, autosomal dominant 24",
            "description": ""
        },
        {
            "id": "MONDO:0014357",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014357",
            "name": "autosomal dominant mental retardation 24",
            "description": ""
        },
        {
            "id": "MIM:615828",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/615828",
            "name": "Vulto-van Silfout-de Vries syndrome",
            "description": "Vulto-van Silfout-de Vries syndrome"
        }
    ]
}