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DO Term : nemaline myopathy 10 [DOID:0110931] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  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.
  • synonyms:
  • NEM10,
  • congenital myopathy 10,
  • 616165,
  • OMIM:616165
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Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents