Showing entry for Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 1

General Disease Information
BXGD Id	BXGD013997
Disease Name	Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 1
Disease CUI Id	C1834846
MeSH Codes	C23   C18   C11   C10
Disease Class Name	Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases; Eye Diseases; Nervous System Diseases
Semantic Type	Disease or Syndrome
Human Phenotype Ontology Id
Human Phenotype Ontology Term
Disease Ontology Id	DOID:630   DOID:7
Disease Ontology Class Name	genetic disease; disease of anatomical entity
Disorder Network	disorder-protein-compound-food associations