Hypopigmentation

About the Disease
Dilution, Pigmentary, also known as hypopigmentation, is related to oculocerebral syndrome with hypopigmentation and tietz albinism-deafness syndrome, and has symptoms including achromia of skin The drugs Fluorouracil and Antimetabolites have been mentioned in the context of this disorder. Affiliated tissues include skin, eye and breast, and related phenotypes are hypopigmentation of hair and hypopigmentation of the fundus

Common Targets
MC1R | KIF13A | PSMB9 | PHF6 | HLA-B | TYR | HLA-DRB1 | G2475 | KITLG | HLA-A | Anandamide membrane transporter (AMT) | KCNQ5 | P2X Receptor (nonspecified subtype) | Sterol O-acyltransferase (ACAT) (nonspecified subtype) | ENPP1 | TFE3 | PSMB8 | SOX10 | USP9X | RAPGEF3 | HLA-C | RHOA | HLA-DQB1 | RAB27A

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