Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (1)
MIM:124500 - VOHWINKEL SYNDROME; VOWNKL

Xenbase Genes: gjb2

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0007422 - keratoderma hereditarium mutilans

Disease Ontology (DO):
DOID:0111339 - Vohwinkel syndrome