DISEASES

Disease-gene associations mined from literature

Human genes for piebaldism

Piebaldism [DOID:3263]

Piebaldism is a rare autosomal dominant disorder of melanocyte development.:867 Common characteristics include a congenital white forelock, scattered normal pigmented and hypopigmented macules and a triangular shaped depigmented patch on the forehead.

Synonyms:  piebaldism,  DOID:3263,  PIEBALD TRAIT,  Partial albinism (disorder),  Partial albinism disorder ...