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].
Key Facts
- Christianson syndrome's instance of is recorded as developmental defect during embryogenesis[2].
- Christianson syndrome's instance of is recorded as rare disease[3].
- Christianson syndrome's instance of is recorded as class of disease[4].
- Christianson syndrome is a type of X-linked intellectual disability[5].
- Christianson syndrome is a type of X-linked cerebellar ataxia[6].
- Christianson syndrome is a type of multiple congenital anomalies/dysmorphic syndrome-intellectual disability[7].
- Christianson syndrome is a type of X-linked dominant disease[8].
- Christianson syndrome's ICD-9-CM is recorded as 759.89[9].
- Christianson syndrome's NCI Thesaurus ID is recorded as C181001[10].
- Christianson syndrome's health specialty is recorded as medical genetics[11].
- Christianson syndrome's genetic association is recorded as SLC9A6[12].
- Christianson syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060825[13].
- Christianson syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0060825[14].
- Christianson syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[15].