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Details of MYO5B gene in Homo sapiens
Disease |
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| Disease |
OMIM id |
| Diarrhea 2, with microvillus atrophy (DIAR2) [MIM:251850]: A disease characterized by onset of intractable life-threatening watery diarrhea during infancy. Two forms are recognized: early-onset microvillus inclusion disease with diarrhea beginning in the neonatal period, and late-onset, with first symptoms appearing after 3 or 4 months of life. Note=The disease is caused by mutations affecting the gene represented in this entry. |
251850 |
Phenotypes
Abdominal symptom, Abnormality of fluid regulation, Abnormality of metabolism/homeostasis, Abnormality of the abdomen, All, Autosomal recessive inheritance, Death, Death in infancy, Dehydration, Diarrhea, Growth abnormality, Growth delay, Malnutrition, Mode of inheritance, Onset and clinical course, Phenotypic abnormality, Protracted diarrhea.
Orthologs in other species |
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| M. musculus |
D. melonogaster |
C. elegans |
S. purpuratus |
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