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Chronic Progressive External Ophthalmoplegia
Chronic progressive external ophthalmoplegia
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Muscular disorders
(22)
Central core disease
Mitochondrial myopathies
Muscular dystrophy
Myopathy
Arthrogryposis
Arthrogryposis
Centronuclear myopathy
Congenital myopathy
Diastasis recti
Inclusion body myositis
Laminopathy
Macrophagic myofasciitis
Metabolic myopathy
Myokmia
Nemaline myopathy
Orofacial myological disorders
Pelvic Floor Muscle Disorder
Polymyositis
Thyrotoxic myopathy
Torticollis
Writer's cramp
X-linked myotubular myopathy
Zenker's degeneration
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Diseases and disorders
(53)
Syndromes
Ophthalmoplegia
Congenital hypomyelination
Camptomelic syndrome
Cystathionine beta-synthase deficiency disease
Cystathionine beta-synthase deficiency disease
Chromosome 9 trisomy
Chromosome 9 tetrasomy 9p
Chromosome 5 trisomy 5p
Visceroptosis
Congenital arthromyodysplasia
Chromosome 5p- syndrome
Pearson syndrome
Pigmentary retinopathy
Cerebrohepatorenal syndrome
Cerebrotendinous xanthomatosis
Melas syndrome
Mitochondrial myopathy-e- ncephalopathy-lactic acidosis
Congenital facial diplegia
Crow-Fukase syndrome
Craniofrontonasal dysplasia
Craniofacial dysostosis
Cerebral gigantism
Leigh syndrome
Third-nerve palsy
Cleidocranial dysplasia
Leber hereditary optic neuropathy
Cerebral abscess
Carnitine deficiency
Mitochondrial diseases
Partial monosomy
Cutis laxa
Complex regional pain syndromes
Miller fisher syndrome
Craniosynostosis
Myoclonus epilepsy
Myasthenia gravis
Cowden syndrome
Keratitis
Blepharoptosis
Internuclear ophthalmoplegia
Chorioretinitis
Costello syndrome
Friedreich's ataxia
Cardiomyopathy
Charcot-Marie Tooth Disease
Optic atrophy
Diplopia
Heart block
Conjunctivitis
Myopathy
Mitochondrial myopathies
Muscular dystrophy
Central core disease
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Mitochondrial diseases
(16)
Kearns-Sayre syndrome
Mitochondrial encephalomyopathies
Neuropathy, ataxia, and retinitis pigmentosa
Ragged red fibers
Diabetes mellitus and deafness
Diabetes mellitus and deafness
Friedreich's ataxia
Leber hereditary optic neuropathy
Leigh syndrome
Melas syndrome
Mitochondrial myopathies
Myoneurogenic gastrointestinal encephalopathy
Nonsyndromic deafness
Pearson syndrome
Progressive external ophthalmoplegia
Threshold expression
Wolfram syndrome
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Genetic disorders
(20)
Deletion (genetics)
Ragged red fibers
Mitochondrial encephalomyopathies
Pearson syndrome
Pigmentary retinopathy
Pigmentary retinopathy
Cerebrohepatorenal syndrome
Cerebrotendinous xanthomatosis
Melas syndrome
Craniofacial dysostosis
Cleidocranial dysplasia
Leber hereditary optic neuropathy
Carnitine deficiency
Muscular dystrophy
Mitochondrial diseases
Partial monosomy
Central core disease
Costello syndrome
Friedreich's ataxia
Charcot-Marie Tooth Disease
Neuropathy, ataxia, and retinitis pigmentosa
more...
Syndromes
(8)
Kearns-Sayre syndrome
Pearson syndrome
Congenital facial diplegia
Crow-Fukase syndrome
Craniofacial dysostosis
Craniofacial dysostosis
Cerebral gigantism
Complex regional pain syndromes
Miller fisher syndrome
more...
Rare diseases
Kearns-Sayre syndrome
Pearson syndrome
Cerebrohepatorenal syndrome
Crow-Fukase syndrome
Cowden syndrome
Ophthalmology
(9)
Ocular myasthenia
Corneal dystrophy
Pigmentary retinopathy
Leber hereditary optic neuropathy
Keratitis
Keratitis
Blepharoptosis
Chorioretinitis
Optic atrophy
Conjunctivitis
more...
Chromosomes
(57)
Chromosome 10
Chromosome 11
Chromosome 18
Chromosome 3
Chromosome 4
Chromosome 4
Chromosome inversion
AZF1
Allosome
Autosome
Centromere
Chromatid
Chromomere
Chromosomal translocation
Chromosome
Chromosome 1 (human)
Chromosome 12 (human)
Chromosome 13 (human)
Chromosome 14 (human)
Chromosome 15 (human)
Chromosome 16 (human)
Chromosome 17 (human)
Chromosome 19 (human)
Chromosome 2 (human)
Chromosome 20 (human)
Chromosome 21 (human)
Chromosome 22 (human)
Chromosome 5 (human)
Chromosome 6 (human)
Chromosome 7 (human)
Chromosome 8 (human)
Chromosome 9 (human)
Chromosome abnormality
Chromosome conformation capture
Chromosome engineering
Chromosome regions
Chromosome segregation
Derivative chromosome
Dicentric chromosome
Dyad (biology)
G banding
Human β-globin locus
Inchrosil
Isochromosome
Karyotype
Lampbrush chromosome
Locus (genetics)
Marker chromosome
Personalized medicine
Proline-Rich Coiled Coil 1
Ring chromosome
Satellite chromosome
Small supernumerary marker chromosome
Subtelomere
Syntelic
Telomere
X chromosome
Y chromosome
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See also
(20)
Heteroplasmic
Mutation
Mtdna
Short stature
Cerebellar diseases
Cerebellar diseases
Campylobacter pylori
Mitochondrial
Camptodactyly
Cerebellar vermis
Parkinsonism
Extraocular muscles
Degeneration
TRNA
Super Nintendo Entertainment System
OMIM
Muscle weakness
Autosomal dominant
Paraneoplastic
Optic disc
Neuromuscular
more...
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