LMOD3

PanelMode of inheritanceDetails
4 panels
R-numbers: R83
Signed-off version 5.21
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Nemaline myopathy 10, OMIM:616165
Component of the following Super Panels:
  • - Hypotonic infant
  • - Other rare neuromuscular disorders
R-numbers: R81
Signed-off version 4.33
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Nemaline myopathy 10, OMIM:616165
Green
in DDG2P
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 3.79
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
NEMALINE MYOPATHY 10, OMIM:616165
R-numbers: R21, R412
Signed-off version 3.122
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Nemaline myopathy 616165