{
    "disease_id": "DOID:0112044",
    "recommended_name": {
        "id": "DOID:0112044",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0112044",
        "name": "non-syndromic X-linked intellectual disability 98",
        "description": "A non-syndromic X-linked intellectual disability characterized by delayed psychomotor development, poor speech, behavioral abnormalities, poor overall growth, dysmorphic facial features, and often early-onset seizures, with males generally more severely affected than females that has_material_basis_in heterozygous or hemizygous mutation in NEXMIF on chromosome Xq13.3."
    },
    "synonyms": [
        {
            "id": "DOID:0112044",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0112044",
            "name": "MRX98",
            "description": ""
        },
        {
            "id": "DOID:0112044",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0112044",
            "name": "X-linked mental retardation 98",
            "description": ""
        },
        {
            "id": "MONDO:0010483",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010483",
            "name": "X-linked intellectual disability, Cantagrel type",
            "description": "An X-linked syndromic intellectual disability characterized by marked neonatal hypotonia, progressive quadriparesia, severely delayed developmental milestones (walking at 3 years of age), gastroesophageal reflux, stereotypic movements of the hands, esotropia and infantile autism."
        },
        {
            "id": "MONDO:0010483",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010483",
            "name": "MRX98",
            "description": ""
        },
        {
            "id": "MONDO:0010483",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010483",
            "name": "X-linked intellectual developmental disorder-98",
            "description": ""
        },
        {
            "id": "MONDO:0010483",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010483",
            "name": "X-linked intellectual disability-98",
            "description": ""
        },
        {
            "id": "MONDO:0010483",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010483",
            "name": "XLID98",
            "description": ""
        },
        {
            "id": "MONDO:0010483",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010483",
            "name": "intellectual disability, X-linked 98",
            "description": ""
        },
        {
            "id": "MONDO:0010483",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010483",
            "name": "intellectual disability, X-linked type 98",
            "description": ""
        },
        {
            "id": "MONDO:0010483",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010483",
            "name": "mental retardation, X-linked 98",
            "description": ""
        },
        {
            "id": "MONDO:0010483",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010483",
            "name": "mental retardation, X-linked type 98",
            "description": ""
        },
        {
            "id": "MIM:300912",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/300912",
            "name": "Intellectual developmental disorder, X-linked 98",
            "description": "Intellectual developmental disorder, X-linked 98"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0112044"
    ],
    "unlinked_id_list": []
}