GénOncoPGxBio
← Gene index

SEMA3A

HGNC ↗

Kallmann syndrome — HH16 (MIM#614897)

1 article(s) in the watch · Constitutional genetics

Curated publications

7/10

Identification and Functional Characterization of a Novel SEMA3A Exon Deletion Variant in Kallmann Syndrome

Kallmann syndrome — HH16 (MIM#614897)

Gén.22 April 2026

External references

OMIM ↗GeneReviews ↗ClinVar ↗NCBI Gene ↗

Automatic aggregation page — a clinical introduction may be added.