congenital diarrhea 6
congenital diarrhea characterized by mild, early-onset chronic diarrhea that has material basis in heterozygous mutation in the GUCY2C gene on chromosome 12p12
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congenital diarrhea 6
Summary
congenital diarrhea 6 is a rare disease[1].
Key Facts
- congenital diarrhea 6's instance of is recorded as rare disease[2].
- congenital diarrhea 6's instance of is recorded as class of disease[3].
- congenital diarrhea 6 is a type of congenital diarrhea[4].
- congenital diarrhea 6 is a type of rare disease involving intestinal motility[5].
- congenital diarrhea 6 is a type of genetic disease[6].
- congenital diarrhea 6 is a type of autosomal dominant disease[7].
- congenital diarrhea 6's symptoms and signs is recorded as diarrhea[8].
- congenital diarrhea 6's genetic association is recorded as GUCY2C[9].
- congenital diarrhea 6's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060780[10].
- congenital diarrhea 6's exact match is recorded as http://identifiers.org/doid/DOID:0060780[11].
- congenital diarrhea 6's on focus list of Wikimedia project is recorded as WikiProject Medicine[12].