Alopecia Universalis Congenita (ALUNC)

Alias:
Alopecia Universalis
Alunc
Atrichia, Generalized
Atrichia Generalized
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Alopecia Universalis Congenita, also known as alopecia universalis, is related to immunodeficiency 41 with lymphoproliferation and autoimmunity and spondyloarthropathy 1. An important gene associated with Alopecia Universalis Congenita is HR (HR Lysine Demethylase And Nuclear Receptor Corepressor), and among its related pathways/superpathways are Innate Immune System and Cytokine Signaling in Immune system. The drugs Prednisolone and Prednisolone acetate have been mentioned in the context of this disorder. Affiliated tissues include skin and thyroid, and related phenotypes are absent eyelashes and absent eyebrow
Related ID:

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
All ages
1-5/10000
19
264
14

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
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