GenTIGSA Gene Database on Rare Genetic Disorders
Congenital Microvillous Atrophy  
Disease Aliases (17)

Congenital familial protracted diarrhea with enterocyte brush-border abnormalities

Congenital familial protracted diarrhoea with enterocyte brush-border abnormalities

Congenital microvillus atrophy

Davidson disease

Diar2

Diarrhea 2 with microvillus atrophy

Diarrhea 2 with microvillus atrophy, with or without cholestasis

Diarrhea with microvillus atrophy 2

Diarrhoea 2 with microvillus atrophy

Microvillous inclusion disease

Microvillus atrophy, congenital

Microvillus inclusion disease

Mvd

Mvid

Myo5b secretory diarrhea

Myo5b secretory diarrhoea

Secretory diarrhea caused by mutation in myo5b

Associated Genes (0)
 

Cross-references of Congenital microvillous atrophy OMIM GARD Orphanet NCBI-GTR NCBI-MedGen MalaCards      MeSH Annotations