Retinal arteriolar tortuosity

Symptom Information:

Symptom ID: HPO:0001136
Synonyms:
Tortuous retinal arterioles [HPO:0001136]
Retinal arteriolar tortuosity [OMIM:Retinal arteriolar tortuosity]
Tortuous retinal arterioles [OMIM:Tortuous retinal arterioles]
Quality:
Cross references:
OMIM: "Retinal arteriolar tortuosity" [OMIM:Retinal arteriolar tortuosity]
OMIM: "Tortuous retinal arterioles" [OMIM:Tortuous retinal arterioles]
Is a (Direct Parents):
HPO         Abnormality of retinal arteries
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the cardiovascular system(HPO:0001626)
          Abnormality of the vasculature(HPO:0002597)
             Abnormality of the systemic arterial tree(HPO:0011004)
                Abnormality of retinal arteries(HPO:0000630)
                   Retinal arteriolar tortuosity(HPO:0001136)
             Abnormality of the vasculature of the eye(HPO:0008047)
                Abnormality of the retinal vasculature(HPO:0008046)
                   Abnormality of retinal arteries(HPO:0000630)
                      Retinal arteriolar tortuosity(HPO:0001136)
       Abnormality of the eye(HPO:0000478)
          Abnormal eye morphology(HPO:0012372)
             Abnormality of the globe(HPO:0012374)
                Abnormality of the posterior segment of the globe(HPO:0004329)
                   Abnormality of the fundus(HPO:0001098)
                      Abnormality of the retina(HPO:0000479)
                         Abnormality of the retinal vasculature(HPO:0008046)
                            Abnormality of retinal arteries(HPO:0000630)
                               Retinal arteriolar tortuosity(HPO:0001136)
                Abnormality of the vasculature of the eye(HPO:0008047)
                   Abnormality of the retinal vasculature(HPO:0008046)
                      Abnormality of retinal arteries(HPO:0000630)
                         Retinal arteriolar tortuosity(HPO:0001136)
MedDRA:
Database Frequency: 5 / 7739
Resource:

All diseases associated with this symptom:

Autosomal dominant familial hematuria - retinal arteriolar tortuosity - contractures (Orphanet:73229)
Familial vascular leukoencephalopathy (Orphanet:36383)
PERICARDIAL EFFUSION, CHRONIC (OMIM:260900)
Retinal arterial tortuosity (Orphanet:75326)
Williams syndrome (Orphanet:904)