9C82.0 Progressive external ophthalmoplegia
International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01
Chronic ophthalmoplegia is characterised by progressive weakness of ocular muscles and levator muscle of the upper eyelid. The condition is mainly manifested in adults. It may be totally and permanently isolated, however in a minority of cases it is associated with skeletal myopathy, which causes abnormal fatigability and even permanent muscle weakness. In this case the affection is still termed isolated progressive external ophthalmoplegia. A large proportion of chronic ophthalmoplegias presents with multisystemic pattern of signs: neurological signs (hearing loss, retinopathy, cerebellar disorders, peripheral neuropathy, etc.), endocrine (diabetes, hypogonadism, hypoparathyroidism, etc.), kidney (kidney failure, tubulopathy, etc.), and heart disorders (conduction disorders, myocardiopathy, etc.).
postcoordination
Add Stem and/or Extension codes to form a cluster code which adds detail to the condition.
Laterality - only one may be selected
synonyms
- Progressive external ophthalmoplegia
- Graefe disease
- PEO - [progressive external ophthalmoplegia]
- ophthalmoplegia plus syndrome
- Chronic progressive external ophthalmoplegia
- CPEO - [Chronic progressive external ophthalmoplegia]
- chronic progressive ophthalmoplegia
- Progressive external ophthalmoplegia, autosomal dominant
- PEOA - [Progressive external ophthalmoplegia, autosomal dominant]
- Progressive external ophthalmoplegia, autosomal dominant, type 1
- PEOA1 - [Progressive external ophthalmoplegia, autosomal dominant, type 1]
- Progressive external ophthalmoplegia, autosomal dominant, type 2
- Progressive external ophthalmoplegia, autosomal dominant, type 3
- PEOA3 - [progressive external ophthalmoplegia, autosomal dominant, type 3]
- Progressive external ophthalmoplegia, autosomal dominant, type 4
- Progressive external ophthalmoplegia, autosomal dominant, type 5
- PEOA5 - [progressive external ophthalmoplegia, autosomal dominant, type 5]
- Progressive external ophthalmoplegia, autosomal recessive
- Kearns-Sayre syndrome
- Kearns-Sayre mitochondrial cytopathy
- Mitochondrial ocular myopathy
- Chronic external ophthalmoplegia, pigmentary degeneration of retina, myopathy and cardiomyopathy
- oculocraniosomatic neuromuscular disorder
- KSS - [Kearns-Sayre syndrome]
- oculocraniosomatic syndrome
- oculocraniosomatic dystrophy
- OCS - [oculocraniosomatic] syndrome
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