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: autosomal dominant disease centronuclear myopathy

autosomal dominant disease centronuclear myopathy Show first 5 Terms
has subtype: centronuclear myopathy 1 centronuclear myopathy 4

centronuclear myopathy 1 centronuclear myopathy 4 Show first 5 Terms

Other Pages

Alliance (1)

Genes Involved

Zebrafish Models