{
    "disease_id": "DOID:0112025",
    "recommended_name": {
        "id": "DOID:0112025",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0112025",
        "name": "female-restricted syndromic X-linked intellectual disability 99",
        "description": "A syndromic X-linked intellectual disability characterized by delayed psychomotor development, mild to moderate intellectual disability, and a wide range of additional congenital anomalies that has_material_basis_in heterozygous mutation in the USP9X gene on chromosome Xp11.4."
    },
    "synonyms": [
        {
            "id": "DOID:0112025",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0112025",
            "name": "MRXS99F",
            "description": ""
        },
        {
            "id": "DOID:0112025",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0112025",
            "name": "X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability",
            "description": ""
        },
        {
            "id": "DOID:0112025",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0112025",
            "name": "female-restricted syndromic X-linked mental retardation 99",
            "description": ""
        },
        {
            "id": "MONDO:0010502",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010502",
            "name": "intellectual disability, X-linked 99, syndromic, female-restricted",
            "description": "Any X-linked syndromic intellectual disability in which the cause of the disease is a mutation in the USP9X gene."
        },
        {
            "id": "MONDO:0010502",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010502",
            "name": "MRXS99F",
            "description": ""
        },
        {
            "id": "MONDO:0010502",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010502",
            "name": "USP9X X-linked syndromic intellectual disability",
            "description": ""
        },
        {
            "id": "MONDO:0010502",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010502",
            "name": "X-linked syndromic intellectual disability caused by mutation in USP9X",
            "description": ""
        },
        {
            "id": "MONDO:0010502",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010502",
            "name": "intellectual developmental disorder, X-linked 99, syndromic, female-restricted, X-linked dominant",
            "description": ""
        },
        {
            "id": "MONDO:0010502",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010502",
            "name": "intellectual disability, X-linked 99, syndromic, female-restricted",
            "description": ""
        },
        {
            "id": "MONDO:0010502",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010502",
            "name": "mental retardation, X-linked 99, syndromic, female-restricted",
            "description": ""
        },
        {
            "id": "MIM:300968",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/300968",
            "name": "Intellectual developmental disorder, X-linked 99, syndromic, female-restricted",
            "description": "Intellectual developmental disorder, X-linked 99, syndromic, female-restricted"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0112025"
    ],
    "unlinked_id_list": []
}