{
    "disease_id": "DOID:0060809", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010355", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010355", 
            "name": "MRXSJ"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010355", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010355", 
            "name": "mental retardation, X-linked, syndromic, Claes-Jensen type; MRXSCJ"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010355", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010355", 
            "name": "mental retardation, X-linked, syndromic, JARID1C-related"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010355", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010355", 
            "name": "mental retardation, X-linked, syndromic, Claes-Jensen type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010355", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010355", 
            "name": "syndromic X-linked intellectual disability due to JARID1C mutation"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010355", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010355", 
            "name": "MRXSCJ"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010355", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010355", 
            "name": "syndromic X-linked mental retardation JARID1C-related"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060809", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060809", 
            "name": "MRXSCJ"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060809", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060809", 
            "name": "MRXSJ"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060809", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060809", 
            "name": "syndromic X-linked intellectual disability due to JARID1C mutation"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060809", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060809", 
            "name": "syndromic X-linked mental retardation JARID1C-related"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060809", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060809", 
            "name": "mental retardation, X-linked, syndromic, Claes-Jensen type"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060809", 
        "description": "A syndromic X-linked intellectual disability characterized by severe intellectual deficit associated with variable clinical manifestations including spasticity, cryptorchidism, maxillary hypoplasia, alopecia areata, epilepsy, short stature, impaired speech and behavioural problems that has_material_basis_in mutation in the KDM5C gene on chromosome Xp11.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060809", 
        "name": "syndromic X-linked intellectual disability Claes-Jensen type"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060809#disease-associations", 
            "id": "0060809", 
            "database": "Alliance of Genome Resources"
        }
    ]
}