Vascular tortuosity
Symptom Information:
Symptom ID: | HPO:0004948 | ||
Synonyms: |
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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 cardiovascular system(HPO:0001626) Abnormality of the vasculature(HPO:0002597) Vascular tortuosity(HPO:0004948) MedDRA: |
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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) |