Skeletal muscle channelopathy (Version: )

Relevant disorders: R76, Myotonia congenita
Signed off date: 22 Mar 2023
Panel types: GMS Rare Disease Virtual, GMS Rare Disease, GMS signed-off
11 green entities
Entity ratingEntityMode of inheritanceMode of pathogenicityTags
Green
BIALLELIC, autosomal or pseudoautosomalN/AN/A
Green
BOTH monoallelic and biallelic, autosomal or pseudoautosomalN/AN/A
Green
BOTH monoallelic and biallelic, autosomal or pseudoautosomalN/AN/A
Green
STRMONOALLELIC, autosomal or pseudoautosomal, NOT imprintedN/ASTR
Green
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknownN/AN/A
Green
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknownN/AN/A
Green
MITOCHONDRIALN/Agene-checked
Green
MITOCHONDRIALN/Agene-checked
Green
BIALLELIC, autosomal or pseudoautosomalN/AN/A
Green
BOTH monoallelic and biallelic, autosomal or pseudoautosomalN/AN/A
Green
BOTH monoallelic and biallelic, autosomal or pseudoautosomalN/AN/A