Abnormality of the vasculature
Symptom Information:
Symptom ID: | HPO:0002597 | ||
Synonyms: |
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Quality: | |||
Cross references: |
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Is a (Direct Parents): | |||
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) MedDRA: |
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Database Frequency: | 5 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Beckwith-Wiedemann syndrome due to CDKN1C mutation | (Orphanet:231120) |
Chuvash erythrocytosis | (Orphanet:238557) |
Glycogen storage disease due to acid maltase deficiency, late-onset | (Orphanet:420429) |
Maturity-onset diabetes of the young, type 3 | (OMIM:600496) |
Polyarteritis nodosa, childhood-onset | (OMIM:615688) |