{
    "disease_id": "DOID:0080226",
    "recommended_name": {
        "id": "DOID:0080226",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0080226",
        "name": "autosomal dominant intellectual developmental disorder 56",
        "description": "An autosomal dominant intellectual developmental disorder that is characterized by global developmental delay, intellectual disability and in most cases hypotonia, delayed walking, poor fine motor skills, and poor or absent speech that has_material_basis_in heterozygous mutation in the CLTC gene on chromosome 17q23."
    },
    "synonyms": [
        {
            "id": "DOID:0080226",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0080226",
            "name": "autosomal dominant mental retardation 56",
            "description": ""
        },
        {
            "id": "DOID:0080226",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0080226",
            "name": "autosomal dominant intellectual developmental disorder-56",
            "description": ""
        },
        {
            "id": "MONDO:0030922",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030922",
            "name": "intellectual disability, autosomal dominant 56",
            "description": ""
        },
        {
            "id": "MONDO:0030922",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030922",
            "name": "CLTC-related ID",
            "description": ""
        },
        {
            "id": "MONDO:0030922",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030922",
            "name": "CLTC-related disorder",
            "description": ""
        },
        {
            "id": "MONDO:0030922",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030922",
            "name": "CLTC-related intellectual disability",
            "description": ""
        },
        {
            "id": "MONDO:0030922",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030922",
            "name": "intellectual disability, autosomal dominant 56",
            "description": ""
        },
        {
            "id": "MONDO:0030922",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030922",
            "name": "MRD56",
            "description": ""
        },
        {
            "id": "MONDO:0030922",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030922",
            "name": "autosomal dominant mental retardation 56",
            "description": ""
        },
        {
            "id": "MONDO:0030922",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030922",
            "name": "mental retardation, autosomal dominant 56",
            "description": ""
        },
        {
            "id": "MIM:617854",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/617854",
            "name": "Intellectual developmental disorder, autosomal dominant 56",
            "description": "Intellectual developmental disorder, autosomal dominant 56"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0080226"
    ],
    "unlinked_id_list": []
}