Severe Congenital Nemaline Myopathy
| Disease Aliases (2) | Severe congenital (neonatal) nm |
Associated Genes (5) NCBI-RefSeq: LMOD3 (Leiomodin 3) External Links: gnomAD browser Ensembl GeneCards
NCBI-RefSeq: KLHL40 (Kelch like family member 40) External Links: gnomAD browser Ensembl GeneCards
NCBI-RefSeq: ACTA1 (Actin alpha 1, skeletal muscle) External Links: gnomAD browser Ensembl GeneCards
NCBI-RefSeq: NEB (Nebulin) External Links: gnomAD browser Ensembl GeneCards
NCBI-RefSeq: KLHL41 (Kelch like family member 41) External Links: gnomAD browser Ensembl GeneCards
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| Cross-references of Severe congenital nemaline myopathy | OMIM | GARD | Orphanet | NCBI-GTR | NCBI-MedGen | MalaCards | MeSH | Annotations | |