ID   HPS2048
AC   CVCL_C9VG
DR   RCB; HPS2048
DR   Wikidata; Q123032027
CC   Donor information: Patient suffering from hemiconvulsion-hemiplegia-epilepsy syndrome, unknown genetic etiology.
CC   Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
DI   NCIt; C3020; Seizure disorder
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
OI   CVCL_C9VH ! HPS2049
OI   CVCL_C9VI ! HPS2050
OI   CVCL_C9VJ ! HPS2051
OI   CVCL_C9VK ! HPS2052
OI   CVCL_C9VL ! HPS2053
SX   Male
AG   6-9Y
CA   Induced pluripotent stem cell
DT   Created: 05-10-23; Last updated: 30-01-24; Version: 2
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