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Human Disease and Mouse Model Detail
Human Disease Waardenburg Syndrome, Type 3; WS3
OMIM ID: 148820
Human Phenotype Ontology associations
Synonyms Klein-Waardenburg Syndrome; Waardenburg Syndrome; Waardenburg Syndrome with Upper Limb Anomalies; Waardenburg Syndrome, Type III
View all models View ALL (5) "NOT" mouse models for this human disease. No mouse models with similarity to the expected human disease phenotype are reported in MGI.
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
     PAX3* Pax3 View 5 "NOT" models 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
MGI 6.07
The Jackson Laboratory