Waardenburg syndrome
Waardenburg syndrome type 2
https://rarediseases.info.nih.gov/diseases/5520/waardenburg-syndrome-type-2
MESH:C536463
WS2
Waardenburg syndrome type 2 (WS2) is an autosomal dominant subtype of Waardenburg syndrome (WS), characterized by varying degrees of deafness and pigmentation anomalies of eyes, hair and skin, but without dystopia canthorum.
WS type 2
Orphanet:895
GARD:5520
UMLS:C2700265
ICD10CM:E70.3
Waardenburg syndrome type 2
WS 2
MONDO:0019517
NCIT:C75009
Waardenburg syndrome type II