{
    "disease_id": "DOID:0112042", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010506", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010506", 
            "name": "intellectual disability, X-linked 61"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010506", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010506", 
            "name": "mental retardation, X-linked 61"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010506", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010506", 
            "name": "MRX61"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010506", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010506", 
            "name": "RLIM non-syndromic X-linked intellectual disability"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010506", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010506", 
            "name": "non-syndromic X-linked intellectual disability caused by mutation in RLIM"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010506", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010506", 
            "name": "mental retardation, X-linked 61; MRX61"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010506", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010506", 
            "name": "mental retardation, X-linked type 61"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010506", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010506", 
            "name": "intellectual disability, X-linked 61; MRX61"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0112042", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0112042", 
            "name": "MRX61"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0112042", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0112042", 
            "name": "TOKAS"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0112042", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0112042", 
            "name": "X-linked mental retardation 61"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0112042", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0112042", 
            "name": "intellectual developmental disorder with or without hand and foot anomalies, genital anomalies, or congenital diaphragmatic hernia"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0112042", 
        "description": "A syndromic X-linked intellectual disability characterized by global developmental delay, impaired intellectual development, speech delay, and behavioral abnormalities in most patients and variable congenital anomalies in some patients that has_material_basis_in mutation in RLIM on chromosome Xq13.2.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0112042", 
        "name": "Tonne-Kalscheuer syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/300978", 
            "id": "300978", 
            "database": "MIM"
        }
    ]
}