{
    "disease_id": "DOID:0060825",
    "recommended_name": {
        "id": "DOID:0060825",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0060825",
        "name": "Christianson syndrome",
        "description": "A syndromic X-linked intellectual disability characterized by microcephaly, impaired ocular movements, progressive severe global developmental delay, developmental regression, hypotonia, abnormal movements, and early-onset seizures of variable types that has_material_basis_in mutation in hemizygous mutation in the SLC9A6 gene on chromosome Xq26."
    },
    "synonyms": [
        {
            "id": "DOID:0060825",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060825",
            "name": "MRXSCH",
            "description": ""
        },
        {
            "id": "DOID:0060825",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060825",
            "name": "X-linked Angelman-like syndrome",
            "description": ""
        },
        {
            "id": "DOID:0060825",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060825",
            "name": "X-linked intellectual disability-craniofacial dysmorphism-epilepsy-ophthalmoplegia-cerebellar atrophy syndrome",
            "description": ""
        },
        {
            "id": "DOID:0060825",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060825",
            "name": "mental retardation, X-linked syndromic, Christianson type",
            "description": ""
        },
        {
            "id": "DOID:0060825",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060825",
            "name": "X-linked intellectual disability, South African type",
            "description": ""
        },
        {
            "id": "DOID:0060825",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060825",
            "name": "mental retardation, microcephaly, epilepsy, and ataxia syndrome",
            "description": ""
        },
        {
            "id": "DOID:0060825",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060825",
            "name": "Christianson type of X-linked syndromic intellectual developmental disorder",
            "description": ""
        },
        {
            "id": "MONDO:0010278",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010278",
            "name": "Christianson syndrome",
            "description": "A very rare form of syndromic intellectual deficit characterized by microcephaly, severe developmental delay or regression, hypotonia, abnormal movements, and early-onset seizures."
        },
        {
            "id": "MONDO:0010278",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010278",
            "name": "Christianson syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010278",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010278",
            "name": "MRXSCH",
            "description": ""
        },
        {
            "id": "MONDO:0010278",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010278",
            "name": "X-linked Angelman-like syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010278",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010278",
            "name": "intellectual developmental disorder, X-linked syndromic, Christianson type",
            "description": ""
        },
        {
            "id": "MONDO:0010278",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010278",
            "name": "intellectual disability, X-linked syndromic, Christianson type",
            "description": ""
        },
        {
            "id": "MONDO:0010278",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010278",
            "name": "intellectual disability, microcephaly, epilepsy, and ataxia syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010278",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010278",
            "name": "mental retardation, microcephaly, epilepsy, and ataxia syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010278",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010278",
            "name": "Angelman-like syndrome X-linked",
            "description": ""
        },
        {
            "id": "MONDO:0010278",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010278",
            "name": "MRXS Christianson",
            "description": ""
        },
        {
            "id": "MONDO:0010278",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010278",
            "name": "X-linked intellectual disability - craniofacial dysmorphism - epilepsy - ophthalmoplegia - cerebellar atrophy",
            "description": ""
        },
        {
            "id": "MONDO:0010278",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010278",
            "name": "intellectual disability X-linked syndromic Christianson type",
            "description": ""
        },
        {
            "id": "MONDO:0010278",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010278",
            "name": "intellectual disability microcephaly epilepsy and ataxia syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010278",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010278",
            "name": "intellectual disability, X-linked, syndromic, Christianson type",
            "description": ""
        },
        {
            "id": "MONDO:0010278",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010278",
            "name": "mental retardation, X-linked, syndromic, Christianson type",
            "description": ""
        },
        {
            "id": "MIM:300243",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/300243",
            "name": "Intellectual developmental disorder, X-linked, syndromic, Christianson type",
            "description": "Intellectual developmental disorder, X-linked, syndromic, Christianson type"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0060825"
    ],
    "unlinked_id_list": []
}