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Entry Name Description Category Pathway Gene
H01372 Vitiligo Vitiligo is a common, multifactorial, polygenic disease in which autoimmune loss of melanocytes results in depigmented spots of skin, overlying hair, and mucous membranes. Some familial forms of vitiligo ... Skin disease (VAMAS1) NLRP1 [HSA:22861] [KO:K12798]
(VAMAS2) FOXD3 [HSA:27022] [KO:K09397]
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