External ophthalmoplegia
Symptom Information:
Symptom ID: | HPO:0000544 | ||||||||||||||||||||||||||||||||||||||||||
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) External ophthalmoplegia(HPO:0000544) MedDRA: Nervous system disorders(MedDRA:10029205) Neurological disorders of the eye(MedDRA:10029301) Ocular signs and symptoms NEC(MedDRA:10030952) External ophthalmoplegia(HPO:0000544) Eye disorders(MedDRA:10015919) Ocular neuromuscular disorders(MedDRA:10030061) Ocular nerve and muscle disorders(MedDRA:10030059) External ophthalmoplegia(HPO:0000544) |
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Database Frequency: | 40 / 7739 | ||||||||||||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
Autosomal dominant centronuclear myopathy | (Orphanet:169189) |
Autosomal recessive spastic paraplegia type 35 | (Orphanet:171629) |
BROWN-VIALETTO-VAN LAERE SYNDROME 1 | (OMIM:211530) |
Biotin-responsive basal ganglia disease | (Orphanet:65284) |
Congenital multicore myopathy with external ophthalmoplegia | (Orphanet:98905) |
Congenital myasthenic syndromes | (Orphanet:590) |
FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 1 | (OMIM:158900) |
Facioscapulohumeral dystrophy | (Orphanet:269) |
Gaucher disease - ophthalmoplegia - cardiovascular calcification | (Orphanet:2072) |
Gaucher disease type 2 | (Orphanet:77260) |
Gaucher disease type 3 | (Orphanet:77261) |
IVIC syndrome | (Orphanet:2307) |
Infantile onset spinocerebellar ataxia | (Orphanet:1186) |
Intellectual deficit, X-linked, Schimke type | (Orphanet:85285) |
Kearns-Sayre syndrome | (Orphanet:480) |
Leigh syndrome | (Orphanet:506) |
Linear nevus sebaceus syndrome | (Orphanet:2612) |
MELAS | (Orphanet:550) |
MYASTHENIA, CONGENITAL, REFRACTORY TO ACETYLCHOLINESTERASE INHIBITORS | (OMIM:254190) |
MYASTHENIC SYNDROME, CONGENITAL, 10 | (OMIM:254300) |
MYASTHENIC SYNDROME, CONGENITAL, 16 | (OMIM:614198) |
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 renal tubulopathy | (Orphanet:255235) |
Mitochondrial DNA depletion syndrome, hepatocerebral form due to DGUOK deficiency | (Orphanet:279934) |
OPHTHALMOPLEGIA, FAMILIAL TOTAL, WITH IRIS TRANSILLUMINATION | (OMIM:165098) |
Oculogastrointestinal muscular dystrophy | (Orphanet:1876) |
Oculopharyngodistal myopathy | (Orphanet:98897) |
Perrault Syndrome 5 | (OMIM:616138) |
Riboflavin transporter deficiency | (Orphanet:97229) |
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 16 | (OMIM:615768) |
Short chain acyl-CoA dehydrogenase deficiency | (Orphanet:26792) |
Spinocerebellar ataxia type 28 | (Orphanet:101109) |
Spinocerebellar ataxia type 3 | (Orphanet:98757) |
Sporadic Leigh syndrome | (Orphanet:255199) |
Thiamine-responsive encephalopathy | (Orphanet:199348) |
Tubular aggregate myopathy | (Orphanet:2593) |
Wolfram syndrome | (Orphanet:3463) |
X-linked centronuclear myopathy | (Orphanet:596) |