ID   PFIZi012-A
AC   CVCL_VE73
SY   FB66c17; RCi198
DR   BioSamples; SAMEA4097192
DR   EBiSC; PFIZi012-A
DR   ECACC; 66540228
DR   hPSCreg; PFIZi012-A
DR   Wikidata; Q54947266
CC   From: Pfizer, Inc.
DI   NCIt; C120408; Chromosome 16p11.2 deletion syndrome
DI   ORDO; Orphanet_261197; Proximal 16p11.2 microdeletion syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens
SX   Sex unspecified
CA   Induced pluripotent stem cell
DT   Created: 14-05-18; Last updated: 12-03-20; Version: 3
//