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 | |