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DO Term : congenital myopathy 5 [DOID:0081341] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A congenital myopathy that is characterized by the onset of muscle weakness in infancy manifest as neonatal hypotonia, delayed motor development, and often distal contractures and that has_material_basis_in homozygous or compound heterozygous mutation in the gene encoding titin (TTN) on chromosome 2q31.
  • synonyms:
  • 611705,
  • congenital myopathy-5 with cardiomyopathy,
  • Salih myopathy,
  • OMIM:611705,
  • ORDO:289377
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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