Genomics England
GMS Panels
Panels
Genes and Entities

LMOD3

leiomodin 3
OMIM: 616112
PanelMode of inheritanceDetails
4 panels
Green
in Arthrogryposis
R-numbers: R83
Signed-off version 7.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Nemaline myopathy 10, OMIM:616165
Green
in Congenital myopathy
Component of the following Super Panels:
  • - Hypotonic infant
  • - Other rare neuromuscular disorders
R-numbers: R81
Signed-off version 4.38
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Nemaline myopathy 10, OMIM:616165
Green
in DDG2P
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 4.6
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
NEMALINE MYOPATHY 10, OMIM:616165
Green
in Fetal anomalies
R-numbers: R21, R412
Signed-off version 4.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Nemaline myopathy 616165