SAMEA1088053

CHDIi021-A

Attributes

Type Value
cell type induced pluripotent stem cell
disease state Huntington disease
material cell line
organism Homo sapiens
phenotype EFO_0004905;Orphanet_399
project EBiSC
sex male
synonym #21c5
synonym CHDI-90002169

Relationships

Source Type Target
SAMEA4675202 derived from SAMEA1088053
SAMEA4675203 derived from SAMEA1088053
SAMEA4675204 derived from SAMEA1088053
SAMEA4675205 derived from SAMEA1088053
SAMEA4675206 derived from SAMEA1088053
SAMEA4675207 derived from SAMEA1088053
SAMEA4675208 derived from SAMEA1088053
SAMEA4675209 derived from SAMEA1088053
SAMEA4675210 derived from SAMEA1088053
SAMEA4675211 derived from SAMEA1088053
SAMEA4675212 derived from SAMEA1088053
SAMEA4675213 derived from SAMEA1088053
SAMEA4675214 derived from SAMEA1088053
SAMEA4675215 derived from SAMEA1088053
SAMEA4675216 derived from SAMEA1088053
SAMEA4675217 derived from SAMEA1088053
SAMEA4675218 derived from SAMEA1088053
SAMEA4675219 derived from SAMEA1088053
SAMEA4675220 derived from SAMEA1088053
SAMEA4675221 derived from SAMEA1088053
SAMEA4675222 derived from SAMEA1088053
SAMEA4675223 derived from SAMEA1088053
SAMEA4675224 derived from SAMEA1088053
SAMEA4675225 derived from SAMEA1088053
SAMEA4675226 derived from SAMEA1088053
SAMEA4675227 derived from SAMEA1088053
SAMEA4675228 derived from SAMEA1088053
SAMEA4675229 derived from SAMEA1088053
SAMEA4675230 derived from SAMEA1088053
SAMEA4675231 derived from SAMEA1088053

External Links

hPSCreg hPSCreg
Released on 2020 / 01 / 09 09:46:46 UTC
Created on 2019 / 11 / 05 09:44:01 UTC
Updated on 2020 / 01 / 09 09:46:49 UTC