FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term nemaline myopathy 10 ID (Ontology) DOID:0110931 (Human Disease)
Definition A nemaline myopathy characterized by early-onset generalized muscle weakness and hypotonia with respiratory insufficiency and feeding difficulties that has_material_basis_in homozygous or compound heterozygous mutation in the LMOD3 gene on chromosome 3p14.
Also Known As "congenital myopathy 10" ; "NEM10"
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 Genes
 nemaline myopathy 10       1
 for disease ribbon | nemaline myopathy 10       1
 model of | nemaline myopathy 10       1
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal recessive disease__
congenital myopathy              |
 |__nemaline myopathy____________|
                                 nemaline myopathy 10  1 rec.
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Is a autosomal recessive disease
nemaline myopathy
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Synonyms
  • "congenital myopathy 10" EXACT
    "NEM10" EXACT OMO:0003012
Secondary IDs
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MIM:616165