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hereditary diarrhea type 2
Genetics:
- associated with defects in MYO5B
Clinical manifestations:
- onset of intractable life-threatening watery diarrhea during infancy
- two forms are recognized:
- early-onset MVID with diarrhea beginning in the neonatal period
- late-onset, with first symptoms appearing after 3 or 4 months of life
General
hereditary diarrhea
secretory diarrhea
Database Correlations
OMIM 251850
References
OMIM :accession 251850