Dowling-Degos Disease 1 (DDD1)

Alias:
Reticular Pigment Anomaly of Flexures
Ddd1
Ddd
Dowling-Degos Disease
Hyperpigmentation
加入收藏
Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Dowling-Degos Disease 1, also known as reticular pigment anomaly of flexures, is related to microphthalmia and pheochromocytoma. An important gene associated with Dowling-Degos Disease 1 is KRT5 (Keratin 5), and among its related pathways/superpathways are Infectious disease and Signal Transduction. The drugs Clindamycin and Desonide have been mentioned in the context of this disorder. Affiliated tissues include skin and breast, and related phenotypes are growth/size/body region and nervous system
Related ID:

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Unknown
--
14
601
17

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