{
    "disease_id": "DOID:0060800", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010574", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010574", 
            "name": "mental retardation, X-linked 59"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010574", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010574", 
            "name": "PGS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010574", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010574", 
            "name": "X-linked metal retardation with Dandy-Walker malformation, basal ganglia disease, and seizures"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010574", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010574", 
            "name": "mental retardation, X-linked, syndromic 21"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010574", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010574", 
            "name": "mental retardation, X-linked, syndromic 5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010574", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010574", 
            "name": "MRX59"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010574", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010574", 
            "name": "syndromic X-linked intellectual disability type 5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010574", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010574", 
            "name": "X-linked mental retardation 59"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010574", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010574", 
            "name": "mental retardation, X-linked, with Dandy-Walker malformation, basal ganglia disease, and seizures"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010574", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010574", 
            "name": "mental retardation X-linked with Dandy-Walker malformation basal ganglia disease and seizures"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010574", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010574", 
            "name": "mental retardation, X-linked, syndromic, fried type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010574", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010574", 
            "name": "syndromic X-linked mental retardation 21"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010574", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010574", 
            "name": "syndromic X-linked mental retardation fried type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010574", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010574", 
            "name": "mental retardation, X-linked syndromic 5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010574", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010574", 
            "name": "fried syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010574", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010574", 
            "name": "Pettigrew syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010574", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010574", 
            "name": "MRXS21"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010574", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010574", 
            "name": "Dandy-Walker malformation with intellectual disability, basal ganglia disease and seizures"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010574", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010574", 
            "name": "X-linked intellectual disability - Dandy-Walker malformation - basal ganglia disease - seizures"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010574", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010574", 
            "name": "X-linked intellectual disability-Dandy-Walker malformation-basal ganglia disease-seizures syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010574", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010574", 
            "name": "MRXS5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010574", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010574", 
            "name": "mental retardation X-linked syndromic 5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010574", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010574", 
            "name": "PETTIGREW syndrome; PGS"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060800", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060800", 
            "name": "X-linked metal retardation with Dandy-Walker malformation, basal ganglia disease, and seizures"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060800", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060800", 
            "name": "Fried syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060800", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060800", 
            "name": "MRX59"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060800", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060800", 
            "name": "MRXS21"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060800", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060800", 
            "name": "Mental retardation, X-linked syndromic 5"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060800", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060800", 
            "name": "Pettigrew syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060800", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060800", 
            "name": "X-linked mental retardation 59"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060800", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060800", 
            "name": "syndromic X-linked mental retardation 21"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060800", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060800", 
            "name": "syndromic X-linked mental retardation Fried type"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060800", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060800", 
            "name": "X-linked intellectual disability-Dandy-Walker malformation-basal ganglia disease-seizures syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060800", 
        "description": "A syndromic X-linked intellectual disability characterized by intellectual disability and variable features including; choreoathetosis, hydrocephalus, Dandy-Walker malformation, seizures, and iron or calcium deposition in the brain that has_material_basis_in mutation in the AP1S2 gene on chromosome Xp22.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060800", 
        "name": "syndromic X-linked intellectual disability 5"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060800#disease-associations", 
            "id": "0060800", 
            "database": "Alliance of Genome Resources"
        }
    ]
}