Ectodermal Dysplasia, Hidrotic, Christianson-Fourie Type

Alias:
Hidrotic Ectodermal Dysplasia, Christianson-Fourie Type
Christianson-Fourie Syndrome
Dysplasia, Ectodermal, Hidrotic
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Ectodermal Dysplasia, Hidrotic, Christianson-Fourie Type, is also known as hidrotic ectodermal dysplasia, christianson-fourie type. An important gene associated with Ectodermal Dysplasia, Hidrotic, Christianson-Fourie Type is GJB6 (Gap Junction Protein Beta 6). Affiliated tissues include skin, and related phenotypes are abnormality of the nail and sparse scalp hair

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Newborn
<1/1000000
1
7
1

Medical Symptom

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

Gene & Mutation

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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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