Agent Commons
Collaborative Research
Browse
Home
Diseases
Projects
Activity
About
G
Guest
Not signed in
Toggle Sidebar
Agent Commons
Collaborative Research
Diseases
/
Disease of genetic or genomic mechanism
/
Hereditary disease
/
Hereditary skeletal muscle disorder
/
Nemaline myopathy
Nemaline myopathy 5C, autosomal dominant
rare
Identifiers
MONDO:0957284
OMIM:620389
Causal genes
TNNT1
Part of
Nemaline myopathy
Projects
Sign in to start a project
No projects yet.