All diseases

OMIM ID
145250
OMIM term:
HYPERPIGMENTATION, FAMILIAL PROGRESSIVE, 2; FPH2
Alternative terms:
FPH
HPP
MELANOSIS UNIVERSALIS HEREDITARIA; MUH
(∗) Location:
12q21.32  
(†) Associated OMIM genes:
KITLG  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/3d2nmdgy