{
    "disease_id": "DOID:0112044", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010483", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010483", 
            "name": "X-linked intellectual disability, Cantagrel type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010483", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010483", 
            "name": "mental retardation, X-linked 98; MRX98"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010483", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010483", 
            "name": "mental retardation, X-linked type 98"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010483", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010483", 
            "name": "MRX98"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010483", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010483", 
            "name": "mental retardation, X-linked 98"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0112044", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0112044", 
            "name": "MRX98"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0112044", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0112044", 
            "name": "X-linked mental retardation 98"
        }, 
        {
            "url": "https://www.omim.org/entry/300912", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:300912", 
            "name": "Mental retardation, X-linked 98"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0112044", 
        "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.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0112044", 
        "name": "non-syndromic X-linked intellectual disability 98"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/300912", 
            "id": "300912", 
            "database": "MIM"
        }
    ]
}