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DO Term : autosomal dominant centronuclear myopathy [DOID:0111217] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A centronuclear myopathy that has_material_basis_in autosomal dominant inheritance.
  • synonyms:
  • ICD10CM:G71.228,
  • SNOMEDCT_US_2023_03_01:716696006,
  • ORDO:169189,
  • UMLS_CUI:C1834558,
  • AD-CNM,
  • MESH:D020914,
  • GARD:12719
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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





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