Amaurosis fugax

Symptom Information:

Symptom ID: HPO:0100576
Synonyms:
Amaurosis fugax (disorder) [Orphanet:5480]
Amaurosis Fugax [Orphanet:5480]
Transient amaurosis/acute visual trouble [Orphanet:5480]
Amaurosis fugax [Orphanet:5480]
Amaurosis fugax [MedDRA:10001903]
Temporary blindness due to vascular insufficiency [MedDRA:10001903]
Amaurosis temporary [MedDRA:10001903]
Quality:
Cross references:
Orphanet:5480 "Transient amaurosis/acute visual trouble" [Orphanet:5480]
UMLS:C0149793 "Amaurosis Fugax" [Orphanet:5480]
Is a (Direct Parents):
Orphanet Abnormality of the eye
MedDRA Transient cerebrovascular events
HPO         Visual impairment
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)
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)