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Disease Ontology Browser
congenital secretory sodium diarrhea 3 (DOID:0060781)
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Synonyms: 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
Alt IDs: OMIM:270420, ICD10CM:P78.3, ORDO:103908
Definition: A secretory diarrhea that has_material_basis_in homozygous or compound heterozygous mutation in the SPINT2 gene on chromosome 19q13.

Disease References using Mouse Models (2)

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)
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last database update
07/05/2024
MGI 6.24
The Jackson Laboratory