{
    "disease_id": "DOID:0060799", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010283", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010283", 
            "name": "MECP2 Duplication syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010283", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010283", 
            "name": "Lubs X-linked mental retardation syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010283", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010283", 
            "name": "Lubs X-linked mental retardation syndrome (formerly)"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010283", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010283", 
            "name": "MRXSL"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010283", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010283", 
            "name": "mental retardation, X-linked, with recurrent respiratory infections"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010283", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010283", 
            "name": "X-linked intellectual disability-hypotonia-recurrent infections syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010283", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010283", 
            "name": "Lubs X-linked mental retardation syndrome; MRXSL"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010283", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010283", 
            "name": "mental retardation, X-linked, Lubs type (formerly)"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010283", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010283", 
            "name": "mental retardation, X-linked, syndromic, Lubs type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010283", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010283", 
            "name": "XLMR syndrome, Lubs type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010283", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010283", 
            "name": "telomeric duplication Xq"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010283", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010283", 
            "name": "distal duplication Xq"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010283", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010283", 
            "name": "trisomy Xq28"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060799", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060799", 
            "name": "mental retardation, X-linked, with recurrent respiratory infections"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060799", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060799", 
            "name": "Lubs X-linked mental retardation syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060799", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060799", 
            "name": "MECP2 duplication syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060799", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060799", 
            "name": "MRXSL"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060799", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060799", 
            "name": "mental retardation, X-linked, syndromic, Lubs type"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060799", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060799", 
            "name": "X-linked intellectual disability-hypotonia-recurrent Infections syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060799", 
        "description": "A syndromic X-linked intellectual disability characterized by moderate to profound intellectual disability, infantile hypotonia, mild dysmorphic features, poor speech development, autistic features, seizures, progressive spasticity, and recurrent infections in males that has_material_basis_in duplication or triplication of the MECP2 gene on chromosome Xq28.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060799", 
        "name": "syndromic X-linked intellectual disability Lubs type"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060799#disease-associations", 
            "id": "0060799", 
            "database": "Alliance of Genome Resources"
        }
    ]
}