ID   HPS2038
AC   CVCL_A3HL
DR   RCB; HPS2038
DR   Wikidata; Q105508408
CC   Sequence variation: Mutation; HGNC; HGNC:1037; CFB; Unexplicit; Not described; Zygosity=Unspecified (RCB=HPS2038).
CC   Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
DI   NCIt; C176902; Atypical hemolytic uremic syndrome-4
DI   ORDO; Orphanet_2134; Atypical hemolytic uremic syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
OI   CVCL_A3HJ ! HPS2036
OI   CVCL_A3HK ! HPS2037
OI   CVCL_A3HM ! HPS2039
OI   CVCL_A3HN ! HPS2040
OI   CVCL_A3HP ! HPS2041
SX   Female
AG   10-19Y
CA   Induced pluripotent stem cell
DT   Created: 12-01-21; Last updated: 19-12-24; Version: 5
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