Search Ontology:
Human Disease

autosomal dominant centronuclear myopathy

Term ID
DOID:0111217
Synonyms
  • AD-CNM
Definition
A centronuclear myopathy that has_material_basis_in autosomal dominant inheritance. https://www.ncbi.nlm.nih.gov/pubmed/30103348
References
  • GARD:12719
  • ICD10CM:G71.228
  • MESH:D020914
  • ORDO:169189
  • SNOMEDCT_US_2023_03_01:716696006
  • UMLS_CUI:C1834558
Ontology
Human Disease   ( DOID:0111217 )
Relationships
is a type of
has subtype
Other Pages
Genes Involved
Zebrafish Models