SAMEA1088031

CHDIi002-A

Released on 2019 / 11 / 05 16:18:50 UTC
Updated on 2019 / 11 / 05 16:18:50 UTC

Attributes

Type Value
Sex male
cell type induced pluripotent stem cell
disease state Huntington disease
material cell line
organism Homo sapiens
phenotype EFO_0004905;Orphanet_399
project EBiSC
synonym #2c3

Relationships

Source Type Target
SAMEA4862113 derived from SAMEA1088031
SAMEA4862114 derived from SAMEA1088031
SAMEA4862115 derived from SAMEA1088031
SAMEA4862116 derived from SAMEA1088031
SAMEA4862117 derived from SAMEA1088031
SAMEA4862118 derived from SAMEA1088031
SAMEA4862119 derived from SAMEA1088031
SAMEA4862120 derived from SAMEA1088031
SAMEA4862121 derived from SAMEA1088031
SAMEA4862122 derived from SAMEA1088031
SAMEA4862123 derived from SAMEA1088031
SAMEA4862124 derived from SAMEA1088031
SAMEA4862125 derived from SAMEA1088031
SAMEA4862126 derived from SAMEA1088031
SAMEA4862127 derived from SAMEA1088031
SAMEA4862128 derived from SAMEA1088031
SAMEA4862129 derived from SAMEA1088031
SAMEA4862130 derived from SAMEA1088031
SAMEA4862131 derived from SAMEA1088031
SAMEA4862132 derived from SAMEA1088031
SAMEA4862133 derived from SAMEA1088031
SAMEA4862134 derived from SAMEA1088031
SAMEA4862135 derived from SAMEA1088031
SAMEA4862136 derived from SAMEA1088031
SAMEA4862137 derived from SAMEA1088031
SAMEA4862138 derived from SAMEA1088031
SAMEA4862139 derived from SAMEA1088031
SAMEA4862140 derived from SAMEA1088031
SAMEA4862141 derived from SAMEA1088031
SAMEA4862142 derived from SAMEA1088031

External Links