Disease #04408 (IMMD (myopathy?, isolated mitochondrial, autosomal dominant(IMMD)), OMIM:616209)

Official abbreviation IMMD
Name myopathy?, isolated mitochondrial, autosomal dominant(IMMD)
OMIM ID 616209
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene CHCHD10
Associated tissues -
Disease features -
Remarks -