Nemaline myopathy 5a, autosomal recessive, severe infantile

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Subtype of: Nemaline myopathy · Nemaline myopathy 5
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Nemaline myopathy 5A, autosomal recessive, severe infantile
MONDO_0011539
TNNT1 Unknown
32994279 10952871
Open Targets
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Nemaline myopathy 5a, autosomal recessive, severe infantile.
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Amish nemaline myopathy 1 shared geneTNNT1 Related via 1 shared gene including TNNT1. Nemaline myopathy 5 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.