Log In|Sign Up
ENActg2 Visceral Myopathy
Alias:
Familial Visceral Myopathy
Hereditary Hollow Visceral Myopathy
Familial Hollow Visceral Myopathy
Megaduodenum and/or Megacystis
Berdon Syndrome
Favorite
Actg2 Visceral Myopathy, also known as familial visceral myopathy, is related to megacystis-microcolon-intestinal hypoperistalsis syndrome 1 and visceral myopathy 1. An important gene associated with Actg2 Visceral Myopathy is ACTG2 (Actin Gamma 2, Smooth Muscle). Affiliated tissues include smooth muscle and thyroid, and related phenotypes are vesicoureteral reflux and hydroureter
Related ID：
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
Medical Symptom
#
Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
Gene & Mutation
#
Gene
Function
Score
Mutations
Related Drugs
Name
CAS Number
Status
Phase
Disease Model
Category
Name
MGI
Related Gene
Strain of Origin
Publications
References Literature
Title
PMID
Journal
Year
IF
