{
    "disease_id": "DOID:0050647", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010533", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010533", 
            "name": "mental retardation, X-linked, syndromic 18"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010533", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010533", 
            "name": "ataxia, fatal X-linked, with deafness and loss of vision"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010533", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010533", 
            "name": "mental retardation, X-linked, syndromic, Arts type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010533", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010533", 
            "name": "MRXSARTS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010533", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010533", 
            "name": "fatal X-linked ataxia with deafness and loss of vision"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010533", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010533", 
            "name": "Arts syndrome; Arts"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010533", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010533", 
            "name": "syndromic X-linked mental retardation 18"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010533", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010533", 
            "name": "Arts"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010533", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010533", 
            "name": "X-linked fatal ataxia with deafness and loss of vision"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010533", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010533", 
            "name": "MRXS18"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010533", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010533", 
            "name": "syndromic X-linked mental retardation Arts type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010533", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010533", 
            "name": "lethal ataxia with deafness and optic atrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010533", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010533", 
            "name": "lethal ataxia-deafness-optic atrophy"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050647", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050647", 
            "name": "fatal X-linked ataxia with deafness and loss of vision"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050647", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050647", 
            "name": "ARTS"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050647", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050647", 
            "name": "Lethal ataxia with deafness and optic atrophy"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050647", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050647", 
            "name": "MRXS18"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050647", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050647", 
            "name": "MRXSARTS"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050647", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050647", 
            "name": "syndromic X-linked mental retardation 18"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050647", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050647", 
            "name": "syndromic X-linked mental retardation Arts type"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0050647", 
        "description": "An X-linked disease that is characterized by profound congenital sensorineural hearing impairment, early-onset hypotonia, delayed motor development, mild to moderate intellectual disability, ataxia, and increased risk of infection and has_material_basis_in mutations of the PRPS1 gene.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0050647", 
        "name": "Arts syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0050647#disease-associations", 
            "id": "0050647", 
            "database": "Alliance of Genome Resources"
        }
    ]
}