Waardenburg syndrome type 2A

Summary
Synonym
  • WS2A
  • Waardenburg syndrome type IIA
Definition
A Waardenburg syndrome characterized by pigmentary abnormalities of the hair, skin, and eyes, congenital sensorineural hearing loss, and absence of lateral displacement of the inner canthus of each eye that has_material_basis_in heterozygous mutation in the MITF gene on chromosome 3p13.
Super Class
Waardenburg syndrome digenic disease
Disease Ontology
DOID:0110950
Mondo Disease Ontology
MeSH
OMIM
GARD
MGI genotype (from TogoID)
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
4286 MITF melanocyte inducing transcription factor
Displaying 1 entry
Gene ID Gene Symbol Description Source
17342 Mitf melanogenesis associated transcription factor

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: December 9, 2024