{
    "disease_id": "DOID:0061035",
    "recommended_name": {
        "id": "DOID:0061035",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0061035",
        "name": "autosomal dominant intellectual developmental disorder 62",
        "description": "An autosomal dominant intellectual developmental disorder that has_material_basis_in caused by heterozygous mutation in the DLG4 gene on chromosome 17p13."
    },
    "synonyms": [
        {
            "id": "MONDO:0032919",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0032919",
            "name": "intellectual developmental disorder 62",
            "description": ""
        },
        {
            "id": "MONDO:0032919",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0032919",
            "name": "DLG4 synaptopathy",
            "description": ""
        },
        {
            "id": "MONDO:0032919",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0032919",
            "name": "DLG4-related synaptopathy",
            "description": ""
        },
        {
            "id": "MONDO:0032919",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0032919",
            "name": "SHINE syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0032919",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0032919",
            "name": "autosomal dominant intellectual developmental disorder-62",
            "description": ""
        },
        {
            "id": "MONDO:0032919",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0032919",
            "name": "intellectual developmental disorder, autosomal dominant 62",
            "description": ""
        },
        {
            "id": "MONDO:0032919",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0032919",
            "name": "sleep disturbances, hypotonia, intellectual disability, neurologic disorder, and epilepsy syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0032919",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0032919",
            "name": "MRD62",
            "description": ""
        },
        {
            "id": "MONDO:0032919",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0032919",
            "name": "Mental Retardation, Autosomal Dominant 62",
            "description": ""
        },
        {
            "id": "MIM:618793",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/618793",
            "name": "Intellectual developmental disorder, autosomal dominant 62",
            "description": "Intellectual developmental disorder, autosomal dominant 62"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0061035"
    ],
    "unlinked_id_list": []
}