Waardenburg syndrome type 2C
MONDO:0011697Mondo
Findings
No curated finding names Waardenburg syndrome type 2C yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
A Waardenburg's 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.
Definition from the Mondo Disease Ontology (MONDO:0011697), read 2026-09-29. CC BY 4.0.
Where it sits
- A kind of
Other names
1 name
Resolves to: Waardenburg syndrome type 2C
- Also called
- WS2C