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CYP17A1
cytochrome P450 family 17 subfamily A member 1
gene with protein product
OMIM: 609300
2 заболевания
GeneCards ↗
Open Targets ↗
NCBI Gene ↗
OMIM ↗
Ассоциированные заболевания
Герминативная мутация (причина)
2
Congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency
ORPHA:90793
→
46,XY difference of sex development due to isolated 17,20-lyase deficiency
ORPHA:90796
→
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Редкие заболевания
CYP17A1
🧬
CYP17A1
cytochrome P450 family 17 subfamily A member 1
gene with protein product
OMIM: 609300
2 заболевания
GeneCards ↗
Open Targets ↗
NCBI Gene ↗
OMIM ↗
Ассоциированные заболевания
Герминативная мутация (причина)
2
Congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency
ORPHA:90793
→
46,XY difference of sex development due to isolated 17,20-lyase deficiency
ORPHA:90796
→