CYP17A1

Partial combined 17α-hydroxylase/17,20-lyase deficiency (46,XY)

1 article(s) in the watch · Constitutional genetics

Curated publications

Genotype-phenotype correlation in partial combined 17α-hydroxylase/17,20-lyase deficiency: functional characterization of CYP17A1 variants in ten 46,XY patients.

Partial combined 17α-hydroxylase/17,20-lyase deficiency (46,XY)

Gén.20 October 2026

External references

OMIM ↗GeneReviews ↗ClinVar ↗NCBI Gene ↗

Automatic aggregation page — a clinical introduction may be added.