Prominent superficial veins
Symptom Information:
Symptom ID: | HPO:0001015 | ||||||
Synonyms: |
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Cross references: |
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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 integument(HPO:0001574) Abnormality of the skin(HPO:0000951) Generalized abnormality of skin(HPO:0011354) Vascular skin abnormality(HPO:0011276) Prominent superficial blood vessels(HPO:0007394) Prominent superficial veins(HPO:0001015) Abnormality of the cardiovascular system(HPO:0001626) Abnormality of the vasculature(HPO:0002597) Venous abnormality(HPO:0002624) Prominent superficial veins(HPO:0001015) MedDRA: |
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Database Frequency: | 7 / 7739 | ||||||
Resource: |
All diseases associated with this symptom:
AREDYLD syndrome | (Orphanet:1133) |
Autosomal recessive severe congenital neutropenia due to G6PC3 deficiency | (Orphanet:331176) |
Familial partial lipodystrophy associated with PPARG mutations | (Orphanet:79083) |
Familial partial lipodystrophy, Dunnigan type | (Orphanet:2348) |
Familial partial lipodystrophy, Köbberling type | (Orphanet:79084) |
Generalized congenital lipodystrophy with myopathy | (Orphanet:228429) |
[DEL] NEUTROPENIA, SEVERE CONGENITAL, 4, AUTOSOMAL RECESSIVE; SCN4 | (OMIM:612541) |