Cohen syndrome

Type

Disease
External link(s)
- Orphanet
- IEMbase
Gene
- VPS13B / VPS13B
  8q22.2
  OMIM
  GnomAD
  Ensembl
  HGNC
  VMH
  LOVD
Gene product
- Vacuolar protein sorting-associated protein 13B
Disease group(s)
- 19.5 Disorders of organelle interplay