Ophthalmoplegia
Symptom Information:
Symptom ID: | HPO:0000602 | |||||||||||||||||||||||||||||||||||||||||
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) Ophthalmoplegia(HPO:0000602) MedDRA: Nervous system disorders(MedDRA:10029205) Neurological disorders of the eye(MedDRA:10029301) Ocular signs and symptoms NEC(MedDRA:10030952) Ophthalmoplegia(HPO:0000602) Eye disorders(MedDRA:10015919) Ocular neuromuscular disorders(MedDRA:10030061) Ocular nerve and muscle disorders(MedDRA:10030059) Ophthalmoplegia(HPO:0000602) |
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Database Frequency: | 56 / 7739 | |||||||||||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
AARSKOG SYNDROME, AUTOSOMAL DOMINANT | (OMIM:100050) |
AL amyloidosis | (Orphanet:85443) |
Aarskog-Scott syndrome | (Orphanet:915) |
Alström syndrome | (Orphanet:64) |
Arthrogryposis with oculomotor limitation and electroretinal anomalies | (Orphanet:1154) |
Atypical Gaucher disease due to saposin C deficiency | (Orphanet:309252) |
Autosomal dominant optic atrophy and congenital deafness | (Orphanet:3212) |
Autosomal recessive centronuclear myopathy | (Orphanet:169186) |
Autosomal recessive spastic paraplegia type 35 | (Orphanet:171629) |
Autosomal recessive spastic paraplegia type 55 | (Orphanet:320375) |
Charcot-Marie-Tooth disease type 4B3 | (Orphanet:363981) |
Christianson syndrome | (Orphanet:85278) |
Combined oxidative phosphorylation defect type 15 | (Orphanet:319524) |
Combined oxidative phosphorylation defect type 7 | (Orphanet:254930) |
Congenital fiber-type disproportion myopathy | (Orphanet:2020) |
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) |
Gordon syndrome | (Orphanet:376) |
Infantile onset spinocerebellar ataxia | (Orphanet:1186) |
Isolated succinate-CoQ reductase deficiency | (Orphanet:3208) |
Kearns-Sayre syndrome | (Orphanet:480) |
Leber plus disease | (Orphanet:99718) |
Leigh syndrome | (Orphanet:506) |
Leukoencephalopathy - thalamus and brainstem anomalies - high lactate | (Orphanet:314051) |
Linear nevus sebaceus syndrome | (Orphanet:2612) |
MELAS | (Orphanet:550) |
MYASTHENIC SYNDROME, CONGENITAL, 10 | (OMIM:254300) |
MYASTHENIC SYNDROME, CONGENITAL, 1A, SLOW-CHANNEL | (OMIM:601462) |
MYASTHENIC SYNDROME, CONGENITAL, 2A, SLOW-CHANNEL | (OMIM:616313) |
MYASTHENIC SYNDROME, CONGENITAL, 3B, FAST-CHANNEL | (OMIM:616322) |
MYASTHENIC SYNDROME, CONGENITAL, 4B, FAST-CHANNEL | (OMIM:616324) |
MYASTHENIC SYNDROME, CONGENITAL, 9, ASSOCIATED WITH ACETYLCHOLINERECEPTOR DEFICIENCY | (OMIM:616325) |
MYOPATHY, CENTRONUCLEAR, 5 | (OMIM:615959) |
MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION | (OMIM:255310) |
Maternally-inherited diabetes and deafness | (Orphanet:225) |
Mitochondrial DNA deletion syndrome with progressive myopathy | (Orphanet:352470) |
Mitochondrial DNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria | (Orphanet:1933) |
NEMALINE MYOPATHY 10 | (OMIM:616165) |
Necrotizing encephalomyelopathy, subacute, of Leigh, adult | (OMIM:161700) |
OPHTHALMOPLEGIA TOTALIS WITH PTOSIS AND MIOSIS | (OMIM:258400) |
OPHTHALMOPLEGIA, EXTERNAL, AND MYOPIA | (OMIM:311000) |
OPHTHALMOPLEGIA, FAMILIAL STATIC | (OMIM:165000) |
OPHTHALMOPLEGIC NEUROMUSCULAR DISORDER WITH ABNORMAL MITOCHONDRIA | (OMIM:258470) |
Oculogastrointestinal muscular dystrophy | (Orphanet:1876) |
Perrault Syndrome 5 | (OMIM:616138) |
Polyarteritis nodosa, childhood-onset | (OMIM:615688) |
Primary localized amyloidosis | (Orphanet:314709) |
Pyruvate dehydrogenase E1-alpha deficiency | (Orphanet:79243) |
Recessive mitochondrial ataxia syndrome | (Orphanet:94125) |
Spinocerebellar ataxia type 2 | (Orphanet:98756) |
Spinocerebellar ataxia type 28 | (Orphanet:101109) |
Sporadic Leigh syndrome | (Orphanet:255199) |
WERNICKE-KORSAKOFF SYNDROME | (OMIM:277730) |
Wolfram syndrome | (Orphanet:3463) |