Ophthalmoparesis
Symptom Information:
Symptom ID: | HPO:0000597 | |||||||||||||||||||||||||||||||||||||||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the eye(HPO:0000478) Abnormal eye physiology(HPO:0012373) Abnormality of eye movement(HPO:0000496) Ophthalmoparesis(HPO:0000597) MedDRA: Eye disorders(MedDRA:10015919) Ocular neuromuscular disorders(MedDRA:10030061) Ocular nerve and muscle disorders(MedDRA:10030059) Ophthalmoparesis(HPO:0000597) Nervous system disorders(MedDRA:10029205) Neurological disorders of the eye(MedDRA:10029301) Ocular signs and symptoms NEC(MedDRA:10030952) Ophthalmoparesis(HPO:0000597) |
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Database Frequency: | 71 / 7739 | |||||||||||||||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
Acetazolamide-responsive myotonia | (Orphanet:99736) |
Arthrogryposis with oculomotor limitation and electroretinal anomalies | (Orphanet:1154) |
Atypical progressive supranuclear palsy | (Orphanet:99750) |
Autosomal dominant cerebellar ataxia | (Orphanet:99) |
Autosomal recessive malignant osteopetrosis | (Orphanet:667) |
Autosomal recessive spastic paraplegia type 35 | (Orphanet:171629) |
Behr syndrome | (Orphanet:1239) |
Carey-Fineman-Ziter syndrome | (Orphanet:1358) |
Centronuclear myopathy | (Orphanet:595) |
Cerebellar ataxia - areflexia - pes cavus - optic atrophy - sensorineural hearing loss | (Orphanet:1171) |
Christianson syndrome | (Orphanet:85278) |
Congenital myasthenic syndromes with glycosylation defect | (Orphanet:353327) |
Crigler-Najjar syndrome | (Orphanet:205) |
Crigler-Najjar syndrome type 1 | (Orphanet:79234) |
Deafness - small bowel diverticulosis - neuropathy | (Orphanet:3217) |
Duane anomaly - myopathy - scoliosis | (Orphanet:50817) |
Duane retraction syndrome | (Orphanet:233) |
Epidermolysis bullosa simplex with muscular dystrophy | (Orphanet:257) |
FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 1 | (OMIM:158900) |
Gaucher disease - ophthalmoplegia - cardiovascular calcification | (Orphanet:2072) |
Gaucher disease type 2 | (Orphanet:77260) |
Gaucher disease type 3 | (Orphanet:77261) |
Generalized epidermolysis bullosa simplex, non-Dowling-Meara type | (Orphanet:79399) |
Giant cell arteritis | (Orphanet:397) |
Horizontal gaze palsy with progressive scoliosis | (Orphanet:2744) |
Hyperkalemic periodic paralysis | (Orphanet:682) |
Infantile onset spinocerebellar ataxia | (Orphanet:1186) |
Intellectual deficit - myopathy - short stature - endocrine defect | (Orphanet:3068) |
Intellectual disability-developmental delay-contractures syndrome | (Orphanet:3454) |
Kearns-Sayre syndrome | (Orphanet:480) |
Leigh syndrome | (Orphanet:506) |
Linear nevus sebaceus syndrome | (Orphanet:2612) |
MELAS | (Orphanet:550) |
MERRF | (Orphanet:551) |
MOTOR NEURON DISEASE WITH DEMENTIA AND OPHTHALMOPLEGIA | (OMIM:600333) |
MYASTHENIC SYNDROME, CONGENITAL, 10 | (OMIM:254300) |
MYASTHENIC SYNDROME, CONGENITAL, 1A, SLOW-CHANNEL | (OMIM:601462) |
MYASTHENIC SYNDROME, CONGENITAL, 1B, FAST-CHANNEL | (OMIM:608930) |
MYASTHENIC SYNDROME, CONGENITAL, 4A, SLOW-CHANNEL | (OMIM:605809) |
MYASTHENIC SYNDROME, CONGENITAL, 4C, ASSOCIATED WITH ACETYLCHOLINERECEPTOR DEFICIENCY | (OMIM:608931) |
MYOPATHY, CENTRONUCLEAR, 1 | (OMIM:160150) |
MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION | (OMIM:255310) |
Macrostomia - preauricular tags - external ophthalmoplegia | (Orphanet:83619) |
Maternally-inherited cardiomyopathy and hearing loss | (Orphanet:1349) |
Maternally-inherited diabetes and deafness | (Orphanet:225) |
Mitochondrial DNA deletion syndrome with progressive myopathy | (Orphanet:352470) |
Moebius syndrome | (Orphanet:570) |
Myasthenia gravis | (Orphanet:589) |
Myotonia fluctuans | (Orphanet:99734) |
Myotonia permanens | (Orphanet:99735) |
Neuronal intranuclear inclusion disease | (Orphanet:2289) |
OSTEOPETROSIS, AUTOSOMAL RECESSIVE 1 | (OMIM:259700) |
Oculogastrointestinal muscular dystrophy | (Orphanet:1876) |
Oculopharyngeal muscular dystrophy | (Orphanet:270) |
Ophthalmoplegia - intellectual deficit - lingua scrotalis | (Orphanet:2743) |
Ophthalmoplegia - myalgia - tubular aggregates | (Orphanet:2742) |
Perrault Syndrome | (Orphanet:2855) |
Phosphoribosylpyrophosphate synthetase superactivity | (Orphanet:3222) |
Postsynaptic congenital myasthenic syndromes | (Orphanet:98913) |
Potassium-aggravated myotonia | (Orphanet:612) |
Presynaptic congenital myasthenic syndromes | (Orphanet:98914) |
Progressive supranuclear palsy - parkinsonism | (Orphanet:240085) |
Proximal tubulopathy - diabetes mellitus - cerebellar ataxia | (Orphanet:3390) |
Retinitis pigmentosa | (Orphanet:791) |
Rhabdoid tumor | (Orphanet:69077) |
Spinocerebellar ataxia type 28 | (Orphanet:101109) |
Sporadic Leigh syndrome | (Orphanet:255199) |
Sudden infant death - dysgenesis of the testes | (Orphanet:168593) |
Synaptic congenital myasthenic syndromes | (Orphanet:98915) |
Wolfram syndrome | (Orphanet:3463) |
X-linked centronuclear myopathy | (Orphanet:596) |