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CYP21A2
cytochrome P450 family 21 subfamily A member 2
gene with protein product
OMIM: 613815
2 заболевания
GeneCards ↗
Open Targets ↗
NCBI Gene ↗
OMIM ↗
Ассоциированные заболевания
Герминативная мутация (причина)
2
Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency, simple virilizing form
ORPHA:315311
→
Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency, salt wasting form
ORPHA:315306
→
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Редкие заболевания
CYP21A2
🧬
CYP21A2
cytochrome P450 family 21 subfamily A member 2
gene with protein product
OMIM: 613815
2 заболевания
GeneCards ↗
Open Targets ↗
NCBI Gene ↗
OMIM ↗
Ассоциированные заболевания
Герминативная мутация (причина)
2
Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency, simple virilizing form
ORPHA:315311
→
Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency, salt wasting form
ORPHA:315306
→