{
    "disease_id": "DOID:0070043",
    "recommended_name": {
        "id": "DOID:0070043",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0070043",
        "name": "autosomal dominant intellectual developmental disorder 13",
        "description": "An autosomal dominant intellectual developmental disorder that has_material_basis_in an autosomal dominant mutation of the DYNC1H1 gene on chromosome 14q32.31."
    },
    "synonyms": [
        {
            "id": "DOID:0070043",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070043",
            "name": "MRD13",
            "description": ""
        },
        {
            "id": "DOID:0070043",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070043",
            "name": "autosomal dominant mental retardation 13",
            "description": ""
        },
        {
            "id": "DOID:0070043",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070043",
            "name": "mental retardation, autosomal dominant 13, with neuronal migration defects",
            "description": ""
        },
        {
            "id": "DOID:0070043",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070043",
            "name": "autosomal dominant non-syndromic intellectual disability 13",
            "description": ""
        },
        {
            "id": "MONDO:0013805",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013805",
            "name": "intellectual disability, autosomal dominant 13",
            "description": "Any autosomal dominant non-syndromic intellectual disability in which the cause of the disease is a mutation in the DYNC1H1 gene."
        },
        {
            "id": "MONDO:0013805",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013805",
            "name": "DYNC1H1 autosomal dominant non-syndromic intellectual disability",
            "description": ""
        },
        {
            "id": "MONDO:0013805",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013805",
            "name": "MRD13",
            "description": ""
        },
        {
            "id": "MONDO:0013805",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013805",
            "name": "autosomal dominant intellectual disability 13",
            "description": ""
        },
        {
            "id": "MONDO:0013805",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013805",
            "name": "autosomal dominant mental retardation 13",
            "description": ""
        },
        {
            "id": "MONDO:0013805",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013805",
            "name": "autosomal dominant non-syndromic intellectual disability caused by mutation in DYNC1H1",
            "description": ""
        },
        {
            "id": "MONDO:0013805",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013805",
            "name": "intellectual disability, autosomal dominant 13",
            "description": ""
        },
        {
            "id": "MONDO:0013805",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013805",
            "name": "intellectual disability, autosomal dominant 13, with neuronal migration defects",
            "description": ""
        },
        {
            "id": "MONDO:0013805",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013805",
            "name": "intellectual disability, autosomal dominant type 13",
            "description": ""
        },
        {
            "id": "MONDO:0013805",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013805",
            "name": "mental retardation, autosomal dominant 13, with neuronal migration defects",
            "description": ""
        },
        {
            "id": "MONDO:0013805",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013805",
            "name": "mental retardation, autosomal dominant type 13",
            "description": ""
        },
        {
            "id": "MONDO:0013805",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013805",
            "name": "autosomal dominant non-syndromic intellectual disability 13",
            "description": ""
        },
        {
            "id": "MONDO:0013805",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013805",
            "name": "intellectual disability, autosomal dominant, 13, with neuronal migration defects",
            "description": ""
        },
        {
            "id": "MONDO:0013805",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013805",
            "name": "mental retardation, autosomal dominant 13",
            "description": ""
        },
        {
            "id": "MONDO:0013805",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013805",
            "name": "mental retardation, autosomal dominant, 13, with neuronal migration defects",
            "description": ""
        },
        {
            "id": "MIM:614563",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/614563",
            "name": "Cortical dysplasia, complex, with other brain malformations 13",
            "description": "Cortical dysplasia, complex, with other brain malformations 13"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0070043"
    ],
    "unlinked_id_list": []
}