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DO Term : nemaline myopathy 8 [DOID:0110930] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A nemaline myopathy characterized by fetal akinesia or hypokinesia, followed by contractures, fractures, respiratory failure, and swallowing difficulties apparent at birth that has_material_basis_in homozygous or compound heterozygous mutation in the KLHL40 gene on chromosome 3p22.
  • synonyms:
  • nemaline myopathy 8, autosomal recessive,
  • 615348,
  • NEM8,
  • OMIM:615348
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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