{
    "disease_id": "DOID:0060825", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010278", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010278", 
            "name": "mental retardation, X-linked syndromic, Christianson type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010278", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010278", 
            "name": "MRXS Christianson"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010278", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010278", 
            "name": "mental retardation, X-linked, syndromic, Christianson type; MRXSCH"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010278", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010278", 
            "name": "X-linked intellectual disability-craniofacial dysmorphism-epilepsy-ophthalmoplegia-cerebellar atrophy syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010278", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010278", 
            "name": "Angelman-like syndrome x-linked"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010278", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010278", 
            "name": "mental retardation, X-linked, syndromic, Christianson type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010278", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010278", 
            "name": "mental retardation, microcephaly, epilepsy, and ataxia syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010278", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010278", 
            "name": "Angelman-like syndrome, X-linked"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010278", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010278", 
            "name": "X-linked Angelman-like syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010278", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010278", 
            "name": "X-linked intellectual disability, South African type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010278", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010278", 
            "name": "MRXSCH"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010278", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010278", 
            "name": "intellectual disability x-linked syndromic Christianson type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010278", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010278", 
            "name": "intellectual disability microcephaly epilepsy and ataxia syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010278", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010278", 
            "name": "X-linked intellectual disability - craniofacial dysmorphism - epilepsy - ophthalmoplegia - cerebellar atrophy"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060825", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060825", 
            "name": "MRXSCH"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060825", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060825", 
            "name": "X-linked Angelman-like syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060825", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060825", 
            "name": "X-linked intellectual disability-craniofacial dysmorphism-epilepsy-ophthalmoplegia-cerebellar atrophy syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060825", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060825", 
            "name": "mental retardation, X-linked syndromic, Christianson type"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060825", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060825", 
            "name": "X-linked intellectual disability, South African type"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060825", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060825", 
            "name": "mental retardation, microcephaly, epilepsy, and ataxia syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060825", 
        "description": "A syndromic X-linked intellectual disability characterized by severe developmental delay, intellectual disability, microcephaly, impaired speech, ataxia, hypotonia and early-onset seizures that has_material_basis_in mutation in the SLC9A6 gene on chromosome Xq26.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060825", 
        "name": "Christianson syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060825#disease-associations", 
            "id": "0060825", 
            "database": "Alliance of Genome Resources"
        }
    ]
}