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
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