congenital adrenal insufficiency Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_0050546)
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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