Gene: CYP21A2 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 1589
Gene Symbol: CYP21A2
CYP21A2 		0.100 CausalMutation group CLINVAR The spectrum of clinical, hormonal and molecular findings in 280 individuals with nonclassical congenital adrenal hyperplasia caused by mutations of the CYP21A2 gene. 25041270 2015
Entrez Id: 1589
Gene Symbol: CYP21A2
CYP21A2 		0.100 CausalMutation group CLINVAR Prevalence of nonclassic congenital adrenal hyperplasia in Turkish children presenting with premature pubarche, hirsutism, or oligomenorrhoea. 24778650 2014
Entrez Id: 1589
Gene Symbol: CYP21A2
CYP21A2 		0.100 CausalMutation group CLINVAR Genotype-phenotype correlation in 1,507 families with congenital adrenal hyperplasia owing to 21-hydroxylase deficiency. 23359698 2013
Entrez Id: 1589
Gene Symbol: CYP21A2
CYP21A2 		0.100 CausalMutation group CLINVAR Association between genotype, clinical presentation, and severity of congenital adrenal hyperplasia: a review. 23692712 2013
Entrez Id: 1589
Gene Symbol: CYP21A2
CYP21A2 		0.100 CausalMutation group CLINVAR Genotype-phenotype correlation in 27 pediatric patients in congenital adrenal hyperplasia due to 21-hydroxylase deficiency in a single center. 24904866 2013
Entrez Id: 1589
Gene Symbol: CYP21A2
CYP21A2 		0.100 CausalMutation group CLINVAR Congenital adrenal hyperplasia. 15964450 2005
Entrez Id: 1589
Gene Symbol: CYP21A2
CYP21A2 		0.100 CausalMutation group CLINVAR Congenital adrenal hyperplasia. 12930931 2003
Entrez Id: 1589
Gene Symbol: CYP21A2
CYP21A2 		0.100 CausalMutation group CLINVAR Congenital adrenal hyperplasia due to 21-hydroxylase deficiency. 10857554 2000
Entrez Id: 1589
Gene Symbol: CYP21A2
CYP21A2 		0.100 CausalMutation group CLINVAR Results of screening 1.9 million Texas newborns for 21-hydroxylase-deficient congenital adrenal hyperplasia. 9521938 1998