Disease #00468 (FPH (hyperpigmentation, progressive, familial (FPH)), OMIM:145250)

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	Curator: Johan T. den Dunnen

Official abbreviation	FPH
Name	hyperpigmentation, progressive, familial (FPH)
OMIM ID	145250
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	KITLG
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-07-21 21:36:41 +02:00 (CEST)
Date last edited	N/A