Waardenburg syndrome type 2B
MONDO:0010841Mondo
Findings
No curated finding names Waardenburg syndrome type 2B yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
- Inheritance
- Autosomal dominant inheritance
HPO, annotations 2026-09-02
Features
6 features
What the disease is reported to present with, and how often among people who have it — never how often a feature means the disease. HPO, annotations 2026-09-02.
- Heterochromia iridisHPOHP:0001100
- 36 of 36 reported patients
- Premature graying of hairHPOHP:0002216
- 36 of 36 reported patients
- Sensorineural hearing impairmentHPOHP:0000407
- 36 of 36 reported patients
- White forelockHPOHP:0002211
- 36 of 36 reported patients
- Abnormal facial shapeHPOHP:0001999
- 0 of 36 reported patients
- TelecanthusHPOHP:0000506
- 0 of 36 reported patients
Where it sits
- A kind of
Other names
1 name
Resolves to: Waardenburg syndrome type 2B
- Also called
- WS2B