adrenal hypoplasia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Developmental hypoplasia of the adrenal glands. (Human Phenotype Ontology, HP_0000835)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000835
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Genes

14 genes associated with the adrenal hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
BMP4 bone morphogenetic protein 4
CDKN1C cyclin-dependent kinase inhibitor 1C (p57, Kip2)
GLI3 GLI family zinc finger 3
ICK intestinal cell (MAK-like) kinase
KIAA0196 KIAA0196
LMNA lamin A/C
MKS1 Meckel syndrome, type 1
NR0B1 nuclear receptor subfamily 0, group B, member 1
NSDHL NAD(P) dependent steroid dehydrogenase-like
PEX1 peroxisomal biogenesis factor 1
SIX3 SIX homeobox 3
TBC1D7 TBC1 domain family, member 7
TBX19 T-box 19
ZMPSTE24 zinc metallopeptidase STE24