Term Name: congenital secretory chloride diarrhea 1
Synonyms: congenital chloride diarrhea finnish type, congenital chloride diarrhoea finnish type, congenital chloridorrhea, congenital secretory chloride diarrhoea 1
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.
Ontology: Human Disease [DOID:0060296]   ( DOID:0060296 )

Relationships
is a type of: autosomal recessive disease physical disorder secretory diarrhea