{
    "disease_id": "DOID:0112034", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010660", 
            "description": "", 
            "resource": "MONDO", 
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            "name": "intellectual disability, X-linked 9"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010660", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010660", 
            "name": "mental retardation, X-linked 9"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010660", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010660", 
            "name": "MRX9"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010660", 
            "description": "", 
            "resource": "MONDO", 
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            "name": "mental retardation, X-linked type 9"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010660", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010660", 
            "name": "non-syndromic X-linked intellectual disability caused by mutation in FTSJ1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010660", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010660", 
            "name": "FTSJ1 non-syndromic X-linked intellectual disability"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010660", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010660", 
            "name": "mental retardation, X-linked 9; MRX9"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010660", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010660", 
            "name": "mental retardation, X-linked 44"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0112034", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0112034", 
            "name": "MRX44"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0112034", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0112034", 
            "name": "MRX9"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0112034", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0112034", 
            "name": "X-linked mental retardation 44"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0112034", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0112034", 
            "name": "X-linked mental retardation 9"
        }, 
        {
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            "description": "", 
            "resource": "MIM", 
            "id": "MIM:309549", 
            "name": "Mental retardation, X-linked 44"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0112034", 
        "description": "A non-syndromic X-linked intellectual disability characterized by nonprogressive intellectual disability that has_material_basis_in hemizygous mutation in FTSJ1 on chromosome Xp11.23.", 
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        "id": "DOID:0112034", 
        "name": "non-syndromic X-linked intellectual disability 9"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/309549", 
            "id": "309549", 
            "database": "MIM"
        }
    ]
}