CPEO

GPTKB entity

Statements (25)
Predicate Object
gptkbp:instanceOf gptkb:disease
gptkbp:affects eye muscles
gptkbp:associatedWith Kearns-Sayre syndrome
Pearson syndrome
gptkbp:category gptkb:mitochondrial_myopathy
muscular dystrophy
gptkbp:cause mitochondrial DNA mutations
nuclear DNA mutations
gptkbp:diagnosedBy genetic testing
muscle biopsy
gptkbp:fullName Chronic Progressive External Ophthalmoplegia
https://www.w3.org/2000/01/rdf-schema#label CPEO
gptkbp:inheritance autosomal dominant
autosomal recessive
mitochondrial inheritance
gptkbp:onset childhood
adulthood
gptkbp:symptom ptosis
difficulty moving eyes
progressive weakness of eye muscles
gptkbp:treatment symptomatic management
eyeglasses with prisms
ptosis surgery
gptkbp:bfsParent gptkb:certified_professional_employer_organizations
gptkbp:bfsLayer 7