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Human Disease
congenital secretory sodium diarrhea 3
- Term ID
- DOID:0060781
- Synonyms
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- congenital secretory sodium diarrhea 3 syndromic
- congenital secretory sodium diarrhea 3 with or without other congenital anomalies
- congenital secretory sodium diarrhoea 3
- congenital secretory sodium diarrhoea 3 syndromic
- congenital secretory sodium diarrhoea 3 with or without other congenital anomalies
- 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
- References
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- ICD10CM:P78.3
- MIM:270420
- ORDO:103908
- Ontology
- Human Disease ( DOID:0060781 )
- is a type of
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