microvillus inclusion disease (Q4293116)

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Human disease
  • Davidson disease
  • MVD
  • congenital familial protracted diarrhea with enterocyte brush-border abnormalities
  • congenital microvillus atrophy
  • diarrhea 2 with microvillus atrophy
  • intractable diarrhea of infancy
  • Microvillous inclusion disease
  • DIARRHEA 2, WITH MICROVILLUS ATROPHY; DIAR2
  • Microvillus Inclusion Disease
  • MVID
  • Microvillus Atrophy, Congenital
  • Congenital microvillous atrophy
  • DIARRHEA 2, WITH MICROVILLUS ATROPHY
  • DIAR2
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Language Label Description Also known as
English
microvillus inclusion disease
Human disease
  • Davidson disease
  • MVD
  • congenital familial protracted diarrhea with enterocyte brush-border abnormalities
  • congenital microvillus atrophy
  • diarrhea 2 with microvillus atrophy
  • intractable diarrhea of infancy
  • Microvillous inclusion disease
  • DIARRHEA 2, WITH MICROVILLUS ATROPHY; DIAR2
  • Microvillus Inclusion Disease
  • MVID
  • Microvillus Atrophy, Congenital
  • Congenital microvillous atrophy
  • DIARRHEA 2, WITH MICROVILLUS ATROPHY
  • DIAR2

Statements

Identifiers

0 references
0 references
MONDO:0009635
 
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