Diplopia
Symptom Information:
Symptom ID: | HPO:0000651 | ||||||||
Synonyms: |
|
||||||||
Quality: | |||||||||
Cross references: |
|
||||||||
Is a (Direct Parents): |
|
||||||||
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 vision(HPO:0000504) Abnormality of binocular vision(HPO:0011514) Diplopia(HPO:0000651) MedDRA: Eye disorders(MedDRA:10015919) Vision disorders(MedDRA:10047518) Visual disorders NEC(MedDRA:10047541) Diplopia(HPO:0000651) |
||||||||
Database Frequency: | 37 / 7739 | ||||||||
Resource: |
All diseases associated with this symptom:
Adult intestinal botulism | (Orphanet:178487) |
Alexander disease | (Orphanet:58) |
Arnold-Chiari malformation type I | (Orphanet:268882) |
Botulism | (Orphanet:1267) |
Camurati-Engelmann disease | (Orphanet:1328) |
Childhood-onset autosomal recessive slowly progressive spinocerebellar ataxia | (Orphanet:284324) |
Classical progressive supranuclear palsy | (Orphanet:240071) |
Episodic ataxia type 3 | (Orphanet:79135) |
Episodic ataxia type 4 | (Orphanet:79136) |
Familial encephalopathy with neuroserpin inclusion bodies | (Orphanet:85110) |
Familial paroxysmal ataxia | (Orphanet:97) |
Fatal familial insomnia | (Orphanet:466) |
Foodborne botulism | (Orphanet:228371) |
Giant cell arteritis | (Orphanet:397) |
Infant botulism | (Orphanet:178478) |
Inhalational botulism | (Orphanet:254504) |
Intestinal botulism | (Orphanet:178481) |
Leber plus disease | (Orphanet:99718) |
Locked-in syndrome | (Orphanet:2406) |
MIGRAINE, FAMILIAL HEMIPLEGIC, 2 | (OMIM:602481) |
MULTIPLE SCLEROSIS, SUSCEPTIBILITY TO | (OMIM:126200) |
MYASTHENIA GRAVIS | (OMIM:254200) |
Malignant atrophic papulosis | (Orphanet:679) |
Mitochondrial DNA deletion syndrome with progressive myopathy | (Orphanet:352470) |
Multiple sclerosis - ichthyosis - factor VIII deficiency | (Orphanet:3151) |
Paroxysmal dystonic choreathetosis with episodic ataxia and spasticity | (Orphanet:53583) |
Pellagra-like skin rash-neurological manifestations | (Orphanet:2837) |
Polyarteritis nodosa, childhood-onset | (OMIM:615688) |
Posterior cortical atrophy | (Orphanet:54247) |
Recessive mitochondrial ataxia syndrome | (Orphanet:94125) |
SUPRANUCLEAR PALSY, PROGRESSIVE, 1 | (OMIM:601104) |
SUPRANUCLEAR PALSY, PROGRESSIVE, 2 | (OMIM:609454) |
Spinocerebellar ataxia type 3 | (Orphanet:98757) |
TERATOMA, PINEAL | (OMIM:273120) |
Thymoma | (Orphanet:99867) |
Toxin-mediated infectious botulism | (Orphanet:230800) |
Wound botulism | (Orphanet:178475) |