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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
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.

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
MGI 6.14
The Jackson Laboratory