{
    "disease_id": "DOID:0060806", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010319", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010319", 
            "name": "MRXSH"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010319", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010319", 
            "name": "MRXE"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010319", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010319", 
            "name": "X-linked intellectual disability, Hedera type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010319", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010319", 
            "name": "mental retardation, X-linked, syndromic, Hedera type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010319", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010319", 
            "name": "mental retardation, X-linked, with epilepsy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010319", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010319", 
            "name": "mental retardation, X-linked, syndromic, Hedera type; MRXSH"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010319", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010319", 
            "name": "X-linked mental retardation with epilepsy"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060806", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060806", 
            "name": "mental retardation, X-linked, syndromic, Hedera type"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060806", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060806", 
            "name": "MRXE"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060806", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060806", 
            "name": "MRXSH"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060806", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060806", 
            "name": "X-linked mental retardation with epilepsy"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060806", 
        "description": "A syndromic X-linked intellectual disability characterized by mild to moderate mental retardation and epilepsy that has_material_basis_in mutation in the ATP6AP2 gene on chromosome Xp11.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060806", 
        "name": "syndromic X-linked intellectual disability Hedera type"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060806#disease-associations", 
            "id": "0060806", 
            "database": "Alliance of Genome Resources"
        }
    ]
}