Log In|Sign Up
ENCongenital Chloride Diarrhea
Alias:
Chloride Diarrhea, Congenital, Finnish Type
Familial Chloride Diarrhea
Diarrhea 1
Favorite
Congenital Chloride Diarrhea, also known as chloride diarrhea, congenital, finnish type, is related to diarrhea 1, secretory chloride, congenital and paternal uniparental disomy of chromosome 7, and has symptoms including diarrhea and watery diarrhea. An important gene associated with Congenital Chloride Diarrhea is SLC26A3 (Solute Carrier Family 26 Member 3). Affiliated tissues include kidney and lung.
Related ID：
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
Medical Symptom
#
Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
Gene & Mutation
#
Gene
Function
Score
Mutations
Related Drugs
Name
CAS Number
Status
Phase
Disease Model
Category
Name
MGI
Related Gene
Strain of Origin
Publications
References Literature
Title
PMID
Journal
Year
IF
