Peeling Skin Syndrome 1 (PSS1)

Alias:
Deciduous Skin
Pss1
Keratolysis Exfoliativa Congenita
Peeling Skin Syndrome Type B
Skin Peeling, Familial Continuous Generalized
Skin Peeling Familial Continuous Generalized
Generalized Peeling Skin Syndrome Type B
Generalized Peeling Skin Disease Type B
Inflammatory Peeling Skin Syndrome
Inflammatory Peeling Skin Disease
Skin, Peeling, Syndrome, Type 1
Peeling Skin Syndrome
Pss Type B
Pss
Favorite
Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Peeling Skin Syndrome 1, also known as deciduous skin, is related to peeling skin syndrome and psoriasis. An important gene associated with Peeling Skin Syndrome 1 is CDSN (Corneodesmosin), and among its related pathways/superpathways is Keratinization. Affiliated tissues include skin and brain, and related phenotypes are pruritus and erythroderma
Related ID:

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
Newborn
<1/1000000
3
8
11

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!
Wechat
Comparison
Al agent
Tutorials
Back to top