About   Help   FAQ
Disease Ontology Browser
congenital secretory chloride diarrhea 1 (DOID:0060296)
Alliance: disease page
Synonyms: congenital chloride diarrhea finnish type; congenital chloride diarrhoea finnish type; congenital chloridorrhea; congenital secretory chloride diarrhoea 1
Alt IDs: OMIM:214700, MESH:C536210, ORDO:53689, UMLS_CUI:C0267662
Definition: A secretory diarrhea characterized by excretion of large amounts of watery stool containing high levels of chloride, resulting in dehydration, hypokalemia, and metabolic alkalosis that has_material_basis_in homozygous mutation in the SLC26A3 gene on chromosome 7q31.

Disease References using Mouse Models (1)
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support. 		last database update
03/18/2025
MGI 6.24 		The Jackson Laboratory