PanelApp (stage)
  1. Genes and Genomic Entities
  2. LMOD1

LMOD1

leiomodin 1
OMIM: 602715, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Amber LMOD1 in Mendeliome


Version 1.1891

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Victorian Clinical Genetics Services
Phenotypes
  • Megacystis-microcolon-intestinal hypoperistalsis syndrome 3, MIM# 619362

Amber LMOD1 in Gastrointestinal neuromuscular disease


Level 2: Gastroenterological disorders
Version 1.24

Component of the following Super Panels:

  • Neuromuscular Superpanel

    		•  review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Amber
    • Royal Melbourne Hospital
    Phenotypes
    • Megacystis-microcolon-intestinal hypoperistalsis syndrome 3, MIM# 619362

    Amber LMOD1 in Fetal anomalies


    Version 1.255

    		review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Amber
    • Genomics England PanelApp
    Phenotypes
    • Megacystis-microcolon-intestinal hypoperistalsis syndrome 3, MIM# 619362