Human genes for piebaldism
Piebaldism [DOID:3263]
An integumentary system disease characterized by congenital absence of melanocytes in areas of the skin and hair that has_material_basis_in heterozygous mutation in either KIT or SNAI2 on chromosome 4q12 or 8q11.21, respectively.
Synonyms: piebaldism, DOID:3263, piebaldisms, Partial albinism, PIEBALD TRAIT ...