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GTR Home > Conditions/Phenotypes > Congenital diarrhea 6

Congenital diarrhea 6

Synonyms
Diarrhea 6
Modes of inheritance
Autosomal dominant inheritance (Orphanet)

Summary

Diarrhea-6 is a relatively mild, early-onset chronic diarrhea that may be associated with increased susceptibility to inflammatory bowel disease, small bowel obstruction, and esophagitis (Fiskerstrand et al., 2012). For a discussion of genetic heterogeneity of diarrhea, see DIAR1 (214700). [from OMIM]

Available tests

15 tests are in the database for this condition.

Clinical tests (15 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

  • Also known as: DIAR6, GC-C, GCC, GUC2C, HSER, MECIL, MUCIL, STAR, GUCY2C
    Summary: guanylate cyclase 2C

Clinical features

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Imported from Human Phenotype Ontology (HPO)

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