{
    "disease_id": "DOID:0060820", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010461", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010461", 
            "name": "mental retardation, X-linked, syndromic, Nascimento type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010461", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010461", 
            "name": "X-linked intellectual disability, Nascimento type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010461", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010461", 
            "name": "MRXSN"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010461", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010461", 
            "name": "mental retardation, X-linked, syndromic 30"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010461", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010461", 
            "name": "mental retardation, X-linked syndromic, Nascimento-type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010461", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010461", 
            "name": "X-linked intellectual disability-nail dystrophy-seizures syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010461", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010461", 
            "name": "mental retardation, X-linked, syndromic, Nascimento type; MRXSN"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060820", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060820", 
            "name": "mental retardation, X-linked syndromic, Nascimento-type"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060820", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060820", 
            "name": "X-linked intellectual disability-nail dystrophy-seizures syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060820", 
        "description": "A syndromic X-linked intellectual disability characterized by intellectual disability with dysmorphic features, including large head, synophrys, prominent supraorbital ridges, almond-shaped and deep-set eyes, large ears, wide mouth, myxedematous appearance, hirsutism, abnormal hair whorls, micropenis, and onychodystrophy that has_material_basis_in mutation in the UBE2A gene on chromosome Xq24.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060820", 
        "name": "syndromic X-linked intellectual disability Nascimento type"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060820#disease-associations", 
            "id": "0060820", 
            "database": "Alliance of Genome Resources"
        }
    ]
}