familial progressive hyperpigmentation
GPTKB entity
Statements (18)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
gptkb:skin
genetic disorder |
| gptkbp:affects |
gptkb:skin
|
| gptkbp:firstDescribed |
1940s
|
| gptkbp:hasFeature |
diffuse or patchy hyperpigmentation
increased melanin in basal layer |
| gptkbp:hasGeneticBasis |
unknown
|
| https://www.w3.org/2000/01/rdf-schema#label |
familial progressive hyperpigmentation
|
| gptkbp:inheritance |
autosomal dominant
|
| gptkbp:OMIM |
145250
|
| gptkbp:onset |
infancy
|
| gptkbp:prevalence |
rare
|
| gptkbp:symptom |
progressive hyperpigmentation
|
| gptkbp:synonym |
gptkb:FPH
familial progressive hypermelanosis |
| gptkbp:bfsParent |
gptkb:KITLG
gptkb:KITLG_gene |
| gptkbp:bfsLayer |
8
|