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Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
Waardenburg syndrome type 2A  
Waardenburg syndrome type 2B 
Waardenburg syndrome type 2C 
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 variation in the chromosome region 8p23. (DO)
Waardenburg syndrome type 2E  
Waardenburg Syndrome Type 2F  

Synonyms
Exact Synonyms: WS2C ;   Waardenburg syndrome type IIC
Primary IDs: MESH:C564684
Alternate IDs: OMIM:606662
Definition Sources: https://www.ncbi.nlm.nih.gov/pubmed/11810298 "DO" "DO", https://www.ncbi.nlm.nih.gov/pubmed/20127975 "DO" "DO"

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