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

Official abbreviation FPHH
Name hyperpigmentation, progressive, familial (FPHH)
OMIM ID 145250
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene KITLG
Associated tissues -
Disease features -
Remarks -
Date created 2014-07-21 21:36:41 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

1 entry on 1 page. Showing entry 1.
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00018553 - PubMed: Wang 2009 6-generation family, 18 affecteds (9F, 9M) - no China - - - - - FPHH - KITLG KITLG 1 18 Johan den Dunnen
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