Search Ontology:

Human Disease

autosomal recessive centronuclear myopathy

Term ID

DOID:0111216

Synonyms

AR-CNM

Definition

A centronuclear myopathy that has_material_basis_in autosomal recessive inheritance. https://www.ncbi.nlm.nih.gov/pubmed/30103348

References

GARD:12718
ORDO:169186

Ontology

Human Disease ( DOID:0111216 )

Relationships

is a type of: autosomal recessive disease centronuclear myopathy

autosomal recessive disease centronuclear myopathy Show first 5 Terms
has subtype: centronuclear myopathy 2 centronuclear myopathy 5 centronuclear myopathy 6 with fiber-type disproportion

centronuclear myopathy 2 centronuclear myopathy 5 centronuclear myopathy 6 with fiber-type disproportion Show first 5 Terms

Other Pages

Alliance (1)

Genes Involved

Zebrafish Models