About   Help   FAQ
Disease Ontology Browser
congenital secretory sodium diarrhea 3 (DOID:0060781)
Alliance: disease page
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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support. 		last database update
11/12/2024
MGI 6.24 		The Jackson Laboratory