Diarrhea 11, Malabsorptive, Congenital (DIAR11)

Alias:
Intractable Diarrhea of Infancy Syndrome
Diar11
Idis
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Diarrhea 11, Malabsorptive, Congenital, also known as intractable diarrhea of infancy syndrome, is related to coronary heart disease 1 and heart disease. An important gene associated with Diarrhea 11, Malabsorptive, Congenital is PERCC1 (Proline And Glutamate Rich With Coiled Coil 1). Affiliated tissues include eye and cortex, and related phenotypes are diarrhea and villous atrophy
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
Unknown
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1
2
3

Medical Symptom

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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

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PMID
Journal
Year
IF
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