{
    "disease_id": "DOID:0070036",
    "recommended_name": {
        "id": "DOID:0070036",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0070036",
        "name": "autosomal dominant intellectual developmental disorder 6",
        "description": "An autosomal dominant intellectual developmental disorder that has_material_basis_in an autosomal dominant mutation of the GRIN2B gene on chromosome 12p13.1."
    },
    "synonyms": [
        {
            "id": "DOID:0070036",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070036",
            "name": "MRD6",
            "description": ""
        },
        {
            "id": "DOID:0070036",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070036",
            "name": "autosomal dominant mental retardation 6",
            "description": ""
        },
        {
            "id": "DOID:0070036",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070036",
            "name": "autosomal dominant non-syndromic intellectual disability 6",
            "description": ""
        },
        {
            "id": "MONDO:0013509",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013509",
            "name": "intellectual disability, autosomal dominant 6",
            "description": "Any autosomal dominant non-syndromic intellectual disability in which the cause of the disease is a mutation in the GRIN2B gene."
        },
        {
            "id": "MONDO:0013509",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013509",
            "name": "GRIN2B encephalopathy",
            "description": ""
        },
        {
            "id": "MONDO:0013509",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013509",
            "name": "GRIN2B-related neurodevelopmental disorder",
            "description": ""
        },
        {
            "id": "MONDO:0013509",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013509",
            "name": "GRIN2B autosomal dominant non-syndromic intellectual disability",
            "description": ""
        },
        {
            "id": "MONDO:0013509",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013509",
            "name": "GRIN2B-related developmental delay, intellectual disability and autism spectrum disorder",
            "description": ""
        },
        {
            "id": "MONDO:0013509",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013509",
            "name": "MRD6",
            "description": ""
        },
        {
            "id": "MONDO:0013509",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013509",
            "name": "autosomal dominant non-syndromic intellectual disability caused by mutation in GRIN2B",
            "description": ""
        },
        {
            "id": "MONDO:0013509",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013509",
            "name": "intellectual developmental disorder, autosomal dominant 6, with or without seizures",
            "description": ""
        },
        {
            "id": "MONDO:0013509",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013509",
            "name": "intellectual disability, autosomal dominant 6",
            "description": ""
        },
        {
            "id": "MONDO:0013509",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013509",
            "name": "intellectual disability, autosomal dominant type 6",
            "description": ""
        },
        {
            "id": "MONDO:0013509",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013509",
            "name": "mental retardation, autosomal dominant type 6",
            "description": ""
        },
        {
            "id": "MONDO:0013509",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013509",
            "name": "mental retardation, autosomal dominant 6",
            "description": ""
        },
        {
            "id": "MONDO:0013509",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013509",
            "name": "mental retardation, autosomal dominant 6, with or without seizures",
            "description": ""
        },
        {
            "id": "MIM:613970",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/613970",
            "name": "Intellectual developmental disorder, autosomal dominant 6, with or without seizures",
            "description": "Intellectual developmental disorder, autosomal dominant 6, with or without seizures"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0070036"
    ],
    "unlinked_id_list": []
}