Amaurosis fugax
Symptom Information:
Symptom ID: | HPO:0100576 | |||||||
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 vision(HPO:0000504) Visual impairment(HPO:0000505) Amaurosis fugax(HPO:0100576) MedDRA: Nervous system disorders(MedDRA:10029205) Central nervous system vascular disorders(MedDRA:10007963) Transient cerebrovascular events(MedDRA:10044376) Amaurosis fugax(HPO:0100576) |
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Database Frequency: | 13 / 7739 | |||||||
Resource: |
All diseases associated with this symptom:
Benign adult familial myoclonic epilepsy | (Orphanet:86814) |
CADASIL | (Orphanet:136) |
Essential thrombocythemia | (Orphanet:3318) |
Giant cell arteritis | (Orphanet:397) |
Hemorrhagic fever - renal syndrome | (Orphanet:340) |
Hughes-Stovin syndrome | (Orphanet:228116) |
Lyme disease | (Orphanet:91546) |
MELAS | (Orphanet:550) |
Malignant atrophic papulosis | (Orphanet:679) |
Metachromatic leukodystrophy | (Orphanet:512) |
Non-polyposis Turcot syndrome | (Orphanet:99817) |
Sneddon syndrome | (Orphanet:820) |
Takayasu arteritis | (Orphanet:3287) |