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CYP21A2

—Cytochrome P450 Family 21 Subfamily A Member 2

Chromosome: 6

Location: 6:32038297-32042321

OMIM: 613815

Ensembl: ENSG00000231852

Official·OMIM:613815 Official·ENSG00000231852

Encodes steroid 21-hydroxylase enzyme. Mutations cause congenital adrenal hyperplasia.

Treatment Roadmap — CYP21A2

Preclinical

Phase 1

Phase 2

Phase 3

Approved

Clinical trials have approximately 10% success rate. This roadmap shows the current status, not guaranteed outcomes.

Associated Diseases

Congenital Adrenal Hyperplasia

Autosomal RecessivePrevalence: 1/15000endocrine

Official·OMIM:201910 Official·ORPHA418

Summary

Clinical Trial

Approved Therapy

Registered Variant