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Human Disease and Mouse Model Detail
Human Disease Vohwinkel Syndrome; VOWNKL
OMIM ID: 124500
Human Phenotype Ontology associations
Synonyms Deafness, Congenital, with Keratopachydermia and Constrictions of Fingers and Toes; Keratoderma Hereditarium Mutilans; KHM; Mutilating Keratoderma
Genes and
mouse models
Mutations in human and/or mouse homologs are associated with this disease

      *Disease is associated/modeled with this Gene or a homolog. More...
      Human Homologs Mouse Homologs Mouse Models Homology Source
     GJB2* Gjb2   HomoloGene and HGNC

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
09/20/2016
MGI 6.05
The Jackson Laboratory