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Intermediate nemaline myopathy

MONDO:0015736

Intermediate nemaline myopathy is a type of nemaline myopathy (NM) that shows features of typical NM in neonates with a more severe progression.

Also known as: Intermediate congenital NM, Intermediate congenital nemaline myopathy

2 clinical trials for this condition and its sub-types, 0 tagged with Intermediate nemaline myopathy itself.

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Where it sits in the disease tree

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Part of

↑ Myopathy (987) ↑ Congenital nervous system disorder (284) ↑ Neuromuscular disease caused by qualitative or quantitative defects of tropomyosin (4) ↑ Neuromuscular disease caused by qualitative or quantitative defects of alpha-actin (2) ↑ Neuromuscular disease caused by qualitative or quantitative defects of nebulin (2)

Sub-types of Intermediate nemaline myopathy

Congenital myopathy 2a, typical, autosomal dominant 0 trials
Congenital myopathy 4B, autosomal recessive 0 trials
Nemaline myopathy 2 0 trials
Nemaline myopathy 9 0 trials

Including sub-types (2) Tagged with Intermediate nemaline myopathy (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.