{
    "disease_id": "DOID:0070066",
    "recommended_name": {
        "id": "DOID:0070066",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0070066",
        "name": "autosomal dominant non-syndromic intellectual disability 36",
        "description": "An autosomal dominant non-syndromic intellectual disability that has_material_basis_in an autosomal dominant mutation of PPP2R1A on chromosome 19q13.41."
    },
    "synonyms": [
        {
            "id": "DOID:0070066",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070066",
            "name": "MRD36",
            "description": ""
        },
        {
            "id": "DOID:0070066",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070066",
            "name": "autosomal dominant mental retardation 36",
            "description": ""
        },
        {
            "id": "MONDO:0014605",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014605",
            "name": "microcephaly-corpus callosum hypoplasia-intellectual disability-facial dysmorphism syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0014605",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014605",
            "name": "mental retardation, autosomal dominant 36; MRD36",
            "description": ""
        },
        {
            "id": "MONDO:0014605",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014605",
            "name": "MRD36",
            "description": ""
        },
        {
            "id": "MONDO:0014605",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014605",
            "name": "mental retardation, autosomal dominant 36",
            "description": ""
        },
        {
            "id": "MONDO:0014605",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014605",
            "name": "autosomal dominant mental retardation 36",
            "description": ""
        },
        {
            "id": "MONDO:0014605",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014605",
            "name": "mental retardation, autosomal dominant type 36",
            "description": ""
        },
        {
            "id": "MONDO:0014605",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014605",
            "name": "autosomal dominant non-syndromic intellectual disability 36",
            "description": ""
        },
        {
            "id": "MIM:616362",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/616362",
            "name": "Intellectual developmental disorder, autosomal dominant 36",
            "description": "Intellectual developmental disorder, autosomal dominant 36"
        }
    ]
}