OBO ID: DOID:0060781 |
Term Name: | congenital secretory sodium diarrhea 3 | Search Ontology: | |
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Definition: | A secretory diarrhea that has_material_basis_in homozygous or compound heterozygous mutation in the SPINT2 gene on chromosome 19q13. https://www.ncbi.nlm.nih.gov/pubmed/19185281 | ||
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Ontology: | Human Disease ( DOID:0060781 ) |
OTHER congenital secretory sodium diarrhea 3 PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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