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Details of MYO5B gene in Homo sapiens
Disease |
|---|
| 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.
