Hyperpigmentation with or Without Hypopigmentation, Familial Progressive (FPHH)

Alias:
Fphh
Melanosis Universalis Hereditaria
Muh
Familial Progressive Hyperpigmentation with or Without Hypopigmentation
Hyperpigmentation, Familial Progressive, 2, Formerly
Hyperpigmentation with or Without Hypopigmentation
Familial Progressive Hyper- and Hypopigmentation
Hyperpigmentation, Progressive, Familial
Hyperpigmentation, Familial Progressive
Fph2, Formerly
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Hyperpigmentation with or Without Hypopigmentation, Familial Progressive, also known as fphh, is related to lentigines and familial progressive hyperpigmentation. An important gene associated with Hyperpigmentation with or Without Hypopigmentation, Familial Progressive is KITLG (KIT Ligand), and among its related pathways/superpathways are Pleural mesothelioma and Pluripotent stem cell differentiation pathway. Affiliated tissues include skin.

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Newborn
<1/1000000
10
248
9

Medical Symptom

#
Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

#
Gene
Function
Score
Mutations
No data available

Related Drugs

Name
CAS Number
Status
Phase
No data available

Disease Model

Category
Name
MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

Title
PMID
Journal
Year
IF
No Data Found!
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