ZFIN Human Disease: autosomal dominant centronuclear myopathy

OBO ID: DOID:0111217

Term Name:	autosomal dominant centronuclear myopathy		Search Ontology:
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 autosomal dominant centronuclear myopathy PAGES

Alliance (1)

GENES INVOLVED No data available

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None