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Hereditary Hollow Viscus Myopathy: Disease Bioinformatics

Hereditary Hollow Viscus Myopathy is a digestive disorder leading to intestinal pseudo obstruction. This is a  digestive disorder where the intestines are unable to contract normally and push food through the digestive system, resulting in an obstruction. The walls of the affected gastrointestinal tract becomes thin and the muscles that control its motion start to degenerate. The exact cause of Hereditary Hollow Viscus Myopathy is currently unknown. Symptoms include constipation, vomiting, diarrhea, urological abnormalities, short or dilated small bowel, and failure to thrive. Hereditary Hollow Viscus Myopathy is characterized by impaired function of enteric smooth muscle cells resulting in abnormal intestinal mobility, severe abdominal pain, malnutrition, and even death. Treatment options include surgical ileostomy.

Hereditary Hollow Viscus Myopathy Bioinformatics Tool

Laverne is a handy bioinformatics tool to help facilitate scientific exploration of related genes, diseases and pathways based on co-citations. Explore more on Hereditary Hollow Viscus Myopathy below! For more information on how to use Laverne, please read the How to Guide.
Vizit™, under license from BioVista Inc.

Top Research Reagents

We have 7 products for the study of Hereditary Hollow Viscus Myopathy that can be applied to Western Blot from our catalog of antibodies and ELISA kits.

H00000072-D01P
Western Blot: actin, gamma 2 Antibody [H00000072-D01P] - Analysis of ACTG2 expression in transfected 293T cell line by ACTG2 polyclonal antibody.Lane 1: ACTG2 transfected lysate(41.90 KDa).Lane 2: Non-transfected lysate.

Rabbit Polyclonal
Species Human
Applications WB

1 Publication

Related Genes

Hereditary Hollow Viscus Myopathy has been researched against:

Related Pathways

Hereditary Hollow Viscus Myopathy has been linked to:

Alternate Names

Hereditary Hollow Viscus Myopathy is also known as Familial Visceral Myopathy.