ID   HPS1628
AC   CVCL_YS37
SY   BRCi019-B
DR   hPSCreg; BRCi019-B
DR   RCB; HPS1628
DR   Wikidata; Q94219801
CC   Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
DI   NCIt; C2989; 22q11.2 deletion syndrome
DI   ORDO; Orphanet_567; 22q11.2 deletion syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
OI   CVCL_YS36 ! HPS1627
OI   CVCL_YS38 ! HPS1629
OI   CVCL_YS39 ! HPS1630
OI   CVCL_YS40 ! HPS1631
SX   Female
AG   <10Y
CA   Induced pluripotent stem cell
DT   Created: 12-03-20; Last updated: 29-06-23; Version: 5
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