has material basis in germline mutation in MYO5B secretory diarrhea microvillus inclusion disease https://www.malacards.org/card/diarrhea_2_with_microvillus_atrophy_with_or_without_cholestasis https://www.malacards.org/card/microvillus_inclusion_disease Davidson's disease intractable diarrhoea of infancy MYO5B secretory diarrhoea icd11.foundation:2137578537 Orphanet:2290 secretory diarrhea caused by mutation in MYO5B MYO5B secretory diarrhea GARD:0007039 NORD:1446 congenital microvillus atrophy congenital familial protracted diarrhoea diarrhoea 2 with microvillus atrophy congenital microvillous atrophy NANDO:2100255 diarrhea 2, with microvillus atrophy Microvillus inclusion disease (MVID) is a very rare, severe, malabsorbative syndrome characterized clinically by protracted or intractable neonatal secretory diarrhea and histologically by inclusion bodies on the intestinal epithelium. MONDO:0009635 Davidson disease DIAR2 microvillus inclusion disease MEDGEN:137954 congenital familial protracted diarrhoea with enterocyte brush-border abnormalities microvillous inclusion disease SCTID:235729009 secretory diarrhoea caused by mutation in MYO5B MVID familial enteropathy, microvillus OMIM:251850 UMLS:C0341306 DOID:0060775 congenital familial protracted diarrhoea with enterocyte Brush-border abnormalities congenital familial protracted diarrhea congenital familial protracted diarrhea with enterocyte brush-border abnormalities ICD9:579.8 NANDO:2200913 MedDRA:10068494 diarrhoea 2, with microvillus atrophy congenital secretory diarrhea