ID   HPS3258
AC   CVCL_D1BH
DR   RCB; HPS3258
DR   Wikidata; Q123032582
CC   Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
DI   NCIt; C84738; Glycogen storage disease type V
DI   ORDO; Orphanet_368; Glycogen storage disease due to muscle glycogen phosphorylase deficiency
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
OI   CVCL_D1BD ! HPS3254
OI   CVCL_D1BE ! HPS3255
OI   CVCL_D1BF ! HPS3256
OI   CVCL_D1BG ! HPS3257
OI   CVCL_D1BI ! HPS3259
SX   Male
AG   70-79Y
CA   Induced pluripotent stem cell
DT   Created: 05-10-23; Last updated: 30-01-24; Version: 2
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