{
    "disease_id": "DOID:0050764", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010284", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010284", 
            "name": "MRXSA"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010284", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010284", 
            "name": "Armfield X-linked mental retardation syndrome; MRXSA"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010284", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010284", 
            "name": "mental retardation syndrome, X-linked, Armfield type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010284", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010284", 
            "name": "X-linked intellectual disability, Armfield type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010284", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010284", 
            "name": "mental retardation, X-linked, syndromic, Armfield type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010284", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010284", 
            "name": "Armfield X-linked mental retardation syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010284", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010284", 
            "name": "syndromic X-linked mental retardation Armfield type"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050764", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050764", 
            "name": "Armfield X-linked mental retardation syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050764", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050764", 
            "name": "mental retardation syndrome, X-linked, Armfield type"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050764", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050764", 
            "name": "MRXSA"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050764", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050764", 
            "name": "X-linked intellectual disability, Armfield type"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050764", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050764", 
            "name": "syndromic X-linked mental retardation Armfield type"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0050764", 
        "description": "A syndromic X-linked intellectual disability characterized by intellectual disability, short stature, seizures, and small hands and feet  and in some cases cleft palate or cataracts/glaucoma that has_material_basis_in variation in the chromosomal region Xq28.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0050764", 
        "name": "Armfield syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0050764#disease-associations", 
            "id": "0050764", 
            "database": "Alliance of Genome Resources"
        }
    ]
}