Disease #05756 (CNM6 (myopathy, centronuclear, type 6, with fiber-type disproportion (CNM6)), OMIM:617760)

Official abbreviation CNM6
Name myopathy, centronuclear, type 6, with fiber-type disproportion (CNM6)
OMIM ID 617760
Human Phenotype Ontology Project (HPO) HPO
Inheritance AR
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene MAP3K20
Associated tissues -
Disease features -
Remarks -