Nemaline myopathy 5

Log in to bookmark this disease

Bookmark This Disease

Subtype of: Nemaline myopathy
Show the subtypes
Download as CSV Download as PDF
Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
nemaline myopathy 5
C1854380MESH:C538397MONDO:0011539
TNNT1 Causal — ClinGen
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with Nemaline myopathy 5.
5 View disease cluster →
Amish nemaline myopathy 1 shared geneTNNT1 Related via 1 shared gene including TNNT1. Nemaline myopathy 5a, autosomal recessive, severe infantile 1 shared geneTNNT1 Related via 1 shared gene including TNNT1. Nemaline myopathy 5c, autosomal dominant 1 shared geneTNNT1 Related via 1 shared gene including TNNT1. Childhood-onset nemaline myopathy 1 shared geneTNNT1 Related via 1 shared gene including TNNT1. Nemaline myopathy 1 shared geneTNNT1 Related via 1 shared gene including TNNT1.