Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (0)
MIM:145250 - HYPERPIGMENTATION WITH OR WITHOUT HYPOPIGMENTATION, FAMILIAL PROGRESSIVE; FPHH

Xenbase Genes: kitlg

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0007771 - epidermis gland
MONDO:0013648 - familial progressive hyperpigmentation
MONDO:0017239 - familial progressive hyper- and hypopigmentation

Disease Ontology (DO):
DOID:0111373 - familial progressive hyperpigmentation with or without hypopigmentation