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FGFR3

HGNC ↗

FGFR3-related skeletal dysplasias (Muenke syndrome, hypochondroplasia)

1 article(s) in the watch · Constitutional genetics

Curated publications

6/10

Population-based genomic screening of FGFR3 reveals variant spectrum, disease burden and clinical outcomes in 39,104 newborns.

FGFR3-related skeletal dysplasias (Muenke syndrome, hypochondroplasia)

Gén.27 October 2026

External references

OMIM ↗GeneReviews ↗ClinVar ↗NCBI Gene ↗

Automatic aggregation page — a clinical introduction may be added.