ID   HPS1630
AC   CVCL_YS39
SY   BRCi019-D
DR   hPSCreg; BRCi019-D
DR   RCB; HPS1630
DR   Wikidata; Q94219806
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_YS37 ! HPS1628
OI   CVCL_YS38 ! HPS1629
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
//