Vascular tortuosity

Symptom Information:

Symptom ID: HPO:0004948
Synonyms:
Vascular tortuosity [OMIM:Vascular tortuosity]
Quality:
Cross references:
OMIM: "Vascular tortuosity" [OMIM:Vascular tortuosity]
Is a (Direct Parents):
HPO         Abnormality of the vasculature
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)
             Vascular tortuosity(HPO:0004948)
MedDRA:
Database Frequency: 5 / 7739
Resource:

All diseases associated with this symptom:

Autosomal recessive cutis laxa type 1 (Orphanet:90349)
CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IA (OMIM:219100)
Fabry disease (Orphanet:324)
Leber hereditary optic neuropathy (Orphanet:104)
[DEL] LEBER OPTIC ATROPHY (OMIM:535000)