Diplopia

Symptom Information:

Symptom ID: HPO:0000651
Synonyms:
Double vision [HPO:0000651]
Diplopia (disorder) [Orphanet:5690]
Diplopia [Orphanet:5690]
Diplopia [OMIM:Diplopia]
Diplopia/double vision [Orphanet:5690]
Diplopia [MedDRA:10013036]
Double vision [MedDRA:10013036]
Vision double [MedDRA:10013036]
Quality:
Cross references:
Orphanet:5690 "Diplopia/double vision" [Orphanet:5690]
OMIM: "Diplopia" [OMIM:Diplopia]
UMLS:C0012569 "Diplopia" [HPO:0000651]
UMLS:C0012569 "Diplopia" [Orphanet:5690]
Is a (Direct Parents):
Orphanet Abnormality of the eye
HPO         Abnormality of binocular vision
MedDRA Visual disorders NEC
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)