Diarrhea 4, Malabsorptive, Congenital (DIAR4)

Alias:
Congenital Malabsorptive Diarrhea 4
Enteric Anendocrinosis
Congenital Malabsorptive Diarrhea Due to Paucity of Enteroendocrine Cells
Diar4
Congenital Malabsorptive Diarrhoea Due to Paucity of Enteroendocrine Cells
Diarrhea, Type 4, Malabsorptive, Congenital
Congenital Malabsorptive Diarrhoea 4
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Diarrhea 4, Malabsorptive, Congenital, also known as congenital malabsorptive diarrhea 4, is related to neonatal diabetes and congenital diarrhea, and has symptoms including diarrhea and vomiting. An important gene associated with Diarrhea 4, Malabsorptive, Congenital is NEUROG3 (Neurogenin 3). Affiliated tissues include liver, and related phenotypes are malabsorption and dehydration
Related ID:

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
Newborn
<1/1000000
10
86
1

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!
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