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CSMD2

HGNC ↗

CSMD2-related neurodevelopmental disorder

1 article(s) in the watch · Constitutional genetics

Curated publications

6/10

Haploinsufficiency, de novo and biallelic missense variants in CSMD2 are associated with neurodevelopmental disorders

CSMD2-related neurodevelopmental disorder

Gén.6 October 2026

External references

OMIM ↗GeneReviews ↗ClinVar ↗NCBI Gene ↗

Automatic aggregation page — a clinical introduction may be added.