Christianson syndrome
rare form of syndromic intellectual deficit characterized by microcephaly, severe developmental delay or regression, hypotonia, abnormal movements, and early-onset seizures
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Christianson syndrome
Summary
Christianson syndrome is a developmental defect during embryogenesis[1]. It draws 4 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #133 of 308).[2]
Key Facts
- Christianson syndrome's instance of is recorded as developmental defect during embryogenesis[3].
- Christianson syndrome's instance of is recorded as rare disease[4].
- Christianson syndrome's instance of is recorded as class of disease[5].
- Christianson syndrome's subclass of is recorded as X-linked intellectual disability[6].
- Christianson syndrome's subclass of is recorded as X-linked cerebellar ataxia[7].
- Christianson syndrome's subclass of is recorded as multiple congenital anomalies/dysmorphic syndrome-intellectual disability[8].
- Christianson syndrome's subclass of is recorded as X-linked dominant disease[9].
- Christianson syndrome's MeSH descriptor ID is recorded as C537450[10].
- Christianson syndrome's MeSH descriptor ID is recorded as C567484[11].
- Christianson syndrome's OMIM ID is recorded as 300243[12].
- Christianson syndrome's KEGG ID is recorded as H01914[13].
- Christianson syndrome's Disease Ontology ID is recorded as DOID:0060825[14].
- Christianson syndrome's Orphanet ID is recorded as 85278[15].
- Christianson syndrome's ICD-9-CM is recorded as 759.89[16].
- Christianson syndrome's NCI Thesaurus ID is recorded as C181001[17].
- Christianson syndrome's health specialty is recorded as medical genetics[18].
- Christianson syndrome's genetic association is recorded as SLC9A6[19].
- Christianson syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060825[20].
- Christianson syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0060825[21].
- Christianson syndrome's UMLS CUI is recorded as C2678194[22].
- Christianson syndrome's UMLS CUI is recorded as C1846130[23].
- Christianson syndrome's ICD-10-CM is recorded as Q87.8[24].
- Christianson syndrome's GARD rare disease ID is recorded as 10572[25].
- Christianson syndrome's GARD rare disease ID is recorded as 9155[26].
- Christianson syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[27].
Why It Matters
Christianson syndrome draws 4 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #133 of 308).[2]