{
    "disease_id": "DOID:0060809",
    "recommended_name": {
        "id": "DOID:0060809",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0060809",
        "name": "syndromic X-linked intellectual disability Claes-Jensen type",
        "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 behavioral problems that has_material_basis_in mutation in the KDM5C gene on chromosome Xp11."
    },
    "synonyms": [
        {
            "id": "DOID:0060809",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060809",
            "name": "MRXSCJ",
            "description": ""
        },
        {
            "id": "DOID:0060809",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060809",
            "name": "MRXSJ",
            "description": ""
        },
        {
            "id": "DOID:0060809",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060809",
            "name": "syndromic X-linked intellectual disability due to JARID1C mutation",
            "description": ""
        },
        {
            "id": "DOID:0060809",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060809",
            "name": "syndromic X-linked mental retardation JARID1C-related",
            "description": ""
        },
        {
            "id": "DOID:0060809",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060809",
            "name": "mental retardation, X-linked, syndromic, Claes-Jensen type",
            "description": ""
        },
        {
            "id": "MONDO:0010355",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010355",
            "name": "syndromic X-linked intellectual disability Claes-Jensen type",
            "description": ""
        },
        {
            "id": "MONDO:0010355",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010355",
            "name": "MRXSCJ",
            "description": ""
        },
        {
            "id": "MONDO:0010355",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010355",
            "name": "MRXSJ",
            "description": ""
        },
        {
            "id": "MONDO:0010355",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010355",
            "name": "intellectual developmental disorder, X-linked syndromic, Claes-Jensen type, X-linked recessive",
            "description": ""
        },
        {
            "id": "MONDO:0010355",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010355",
            "name": "intellectual disability, X-linked, syndromic, Claes-Jensen type",
            "description": ""
        },
        {
            "id": "MONDO:0010355",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010355",
            "name": "mental retardation, X-linked, syndromic, Claes-Jensen type",
            "description": ""
        },
        {
            "id": "MONDO:0010355",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010355",
            "name": "syndromic X-linked intellectual disability Claes-Jensen type",
            "description": ""
        },
        {
            "id": "MONDO:0010355",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010355",
            "name": "syndromic X-linked intellectual disability JARID1C-related",
            "description": ""
        },
        {
            "id": "MONDO:0010355",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010355",
            "name": "syndromic X-linked intellectual disability due to JARID1C mutation",
            "description": ""
        },
        {
            "id": "MONDO:0010355",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010355",
            "name": "syndromic X-linked mental retardation JARID1C-related",
            "description": ""
        },
        {
            "id": "MONDO:0010355",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010355",
            "name": "intellectual disability, X-linked, syndromic, JARID1C-related",
            "description": ""
        },
        {
            "id": "MONDO:0010355",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010355",
            "name": "mental retardation, X-linked, syndromic, JARID1C-related",
            "description": ""
        },
        {
            "id": "MIM:300534",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/300534",
            "name": "Intellectual developmental disorder, X-linked, syndromic, Claes-Jensen type",
            "description": "Intellectual developmental disorder, X-linked, syndromic, Claes-Jensen type"
        }
    ]
}