{
    "disease_id": "DOID:0070538",
    "recommended_name": {
        "id": "DOID:0070538",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0070538",
        "name": "syndromic X-linked intellectual developmental disorder bain type",
        "description": "A syndromic X-linked syndromic intellectual disability characterized by delayed psychomotor development, impaired intellectual development with behavioral abnormalities, and musculoskeletal and growth abnormalities that has_material_basis_in heterozygous mutation in the HNRNPH2 gene on chromosome Xq22.1."
    },
    "synonyms": [
        {
            "id": "DOID:0070538",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070538",
            "name": "HNRNPH2-RNDD",
            "description": ""
        },
        {
            "id": "DOID:0070538",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070538",
            "name": "HNRNPH2-related neurodevelopmental disorder",
            "description": ""
        },
        {
            "id": "DOID:0070538",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070538",
            "name": "MRXSB",
            "description": ""
        },
        {
            "id": "DOID:0070538",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070538",
            "name": "Mental Retardation, X-linked, Syndrome, Bain Type",
            "description": ""
        },
        {
            "id": "MONDO:0010512",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010512",
            "name": "intellectual disability, X-linked, syndromic, Bain type",
            "description": ""
        },
        {
            "id": "MONDO:0010512",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010512",
            "name": "MRXSB",
            "description": ""
        },
        {
            "id": "MONDO:0010512",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010512",
            "name": "intellectual developmental disorder, X-linked, syndromic, Bain type, X-linked dominant",
            "description": ""
        },
        {
            "id": "MONDO:0010512",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010512",
            "name": "intellectual disability, X-linked, syndromic, Bain type",
            "description": ""
        },
        {
            "id": "MONDO:0010512",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010512",
            "name": "mental retardation, X-linked, syndromic, Bain type",
            "description": ""
        },
        {
            "id": "MIM:300986",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/300986",
            "name": "Intellectual developmental disorder, X-linked, syndromic, Bain type",
            "description": "Intellectual developmental disorder, X-linked, syndromic, Bain type"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0070538"
    ],
    "unlinked_id_list": []
}