ID   HPS2847
AC   CVCL_YR99
DR   RCB; HPS2847
DR   Wikidata; Q94220294
CC   Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
DI   NCIt; C75463; Prader-Willi syndrome
DI   ORDO; Orphanet_739; Prader-Willi syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
OI   CVCL_UP21 ! HPS2846
OI   CVCL_YS00 ! HPS2848
OI   CVCL_YS01 ! HPS2849
OI   CVCL_YS02 ! HPS2850
OI   CVCL_YS03 ! HPS2851
SX   Female
AG   6-9Y
CA   Induced pluripotent stem cell
DT   Created: 12-03-20; Last updated: 05-10-23; Version: 5
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