Disease #00048

Official abbreviation 610131
Name Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 4, 610131 (3)
OMIM ID 610131
Human Phenotype Ontology Project (HPO) HPO
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene POLG2
Associated tissues -
Disease features -
Remarks -

  Powered by LOVD v.3.0 Build 21
LOVD software ©2004-2018 Leiden University Medical Center