congenital adrenal insufficiency Gene Set
Genes
12 genes co-occuring with the disease congenital adrenal insufficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
| Symbol |
Name |
Standardized Value |
|
STAR
|
steroidogenic acute regulatory protein
|
1.99132
|
|
CYP11A1
|
cytochrome P450, family 11, subfamily A, polypeptide 1
|
1.71226
|
|
FDX1
|
ferredoxin 1
|
1.39171
|
|
FDXR
|
ferredoxin reductase
|
1.19661
|
|
POMC
|
proopiomelanocortin
|
1.04924
|
|
CYP17A1
|
cytochrome P450, family 17, subfamily A, polypeptide 1
|
0.760639
|
|
MC4R
|
melanocortin 4 receptor
|
0.685091
|
|
ARSH
|
arylsulfatase family, member H
|
0.60264
|
|
C4A
|
complement component 4A (Rodgers blood group)
|
0.568386
|
|
LEPR
|
leptin receptor
|
0.439786
|
|
AAAS
|
achalasia, adrenocortical insufficiency, alacrimia
|
0.42139
|
|
GUSB
|
glucuronidase, beta
|
0.349349
|
