ID   HPS2856
AC   CVCL_D0VX
DR   RCB; HPS2856
DR   Wikidata; Q123032431
CC   Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
DI   NCIt; C99026; Protein S deficiency disease
DI   ORDO; Orphanet_743; Severe hereditary thrombophilia due to congenital protein S deficiency
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
OI   CVCL_D0VT ! HPS2852
OI   CVCL_D0VU ! HPS2853
OI   CVCL_D0VV ! HPS2854
OI   CVCL_D0VW ! HPS2855
OI   CVCL_D0VY ! HPS2857
SX   Female
AG   70-79Y
CA   Induced pluripotent stem cell
DT   Created: 05-10-23; Last updated: 30-01-24; Version: 2
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