CSH1

Gene

chorionic somatomammotropin hormone 1

HGNCHGNC:2440 EnsemblENSG00000136488 NCBI Gene1442

Locus: gene with protein productLocation: 17q23.3

Also known as

Symbols and names change; identity (the HGNC ID) does not. Previous and alternative forms are kept distinct.

Also known ashCS-A · CSA · CSMT · FLJ75407 · PL

View full nomenclature history (8)

Alias symbolshCS-A, CSA, CSMT, FLJ75407, PL

Alias namesplacental lactogen, choriomammotropin, chorionic somatomammotropin A

Associated diseases

via associated_with

Diseases linked to this gene through the canonical GENE→DISEASE (associated_with) relation, drawn from Open Targets' top-ranked associations by overall score — not the full association set. Disease-level detail lives on each disease's own page.

46,XX gonadal dysgenesis

Primary Ovarian Insufficiency

Non-acquired isolated growth hormone deficiency

Drawn from Open Targets’ top 10 associations by overall score for this gene — the subset resolved to a canonical disease. Lower-ranked associations, and diseases not yet canonicalised, are not shown.

Gene family

HGNC gene-group membership.

Growth hormone family

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-03-15.

Open TargetsGene–disease associations from the Open Targets Platform.