Diarrhea 1, Secretory Chloride, Congenital (DIAR1)

Alias:
Chloride Diarrhea, Congenital, Finnish Type
Congenital Chloride Diarrhea Finnish Type
Congenital Secretory Chloride Diarrhea 1
Congenital Chloride Diarrhea
Diar1
Diarrhea, Type 1, Chloride, Secretory, Congenital
Congenital Secretory Diarrhea, Chloride Type
Congenital Chloride Diarrhoea Finnish Type
Congenital Secretory Chloride Diarrhoea 1
Diarrhea 1 Secretory Chloride Congenital
Chloridorrhea, Congenital
Congenital Chloridorrhea
Chloridorrhea Congenital
Cld
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Diarrhea 1, Secretory Chloride, Congenital, also known as chloride diarrhea, congenital, finnish type, is related to diarrhea 5, with tufting enteropathy, congenital and diarrhea, and has symptoms including diarrhea and watery diarrhea. An important gene associated with Diarrhea 1, Secretory Chloride, Congenital is SLC26A3 (Solute Carrier Family 26 Member 3), and among its related pathways/superpathways are Transport of inorganic cations/anions and amino acids/oligopeptides and Proximal tubule transport. Related phenotypes are hypokalemia and hyperaldosteronism
Related ID:

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
Unknown
--
8
70
35

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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