Vascular skin abnormality

Symptom Information:

Symptom ID: HPO:0011276
Synonyms:
VASCULAR ABNORMALITIES RESTRICTED TO SKIN [HPO:0011276]
Skin vascular anomaly [Orphanet:23600]
Vascular abnormalities restricted to skin [OMIM:Vascular abnormalities restricted to skin]
Vascular anomalies of skin/mucosae [Orphanet:23600]
Mucosa vascular anomaly [Orphanet:23600]
Skin vascular abnormalities [MedDRA:10047043]
Quality:
Cross references:
Orphanet:23600 "Vascular anomalies of skin/mucosae" [Orphanet:23600]
OMIM: "Vascular abnormalities restricted to skin" [OMIM:Vascular abnormalities restricted to skin]
Is a (Direct Parents):
Orphanet Abnormality of the skin
MedDRA Skin and subcutaneous tissue disorders
HPO         Generalized abnormality of skin
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)
MedDRA:
Skin and subcutaneous tissue disorders(MedDRA:10040785)
    Vascular skin abnormality(HPO:0011276)
Database Frequency: 24 / 7739
Resource:

All diseases associated with this symptom:

Alpha-N-acetylgalactosaminidase deficiency (Orphanet:3137)
Alpha-N-acetylgalactosaminidase deficiency type 1 (Orphanet:79279)
Alpha-N-acetylgalactosaminidase deficiency type 2 (Orphanet:79280)
Angio-osteohypertrophic syndrome (Orphanet:2346)
Angioma serpiginosum (Orphanet:95429)
Aspartylglucosaminuria (Orphanet:93)
Blue rubber bleb nevus (Orphanet:1059)
Cobb syndrome (Orphanet:53721)
Cronkhite-Canada syndrome (Orphanet:2930)
Cutis marmorata telangiectatica congenita (Orphanet:1556)
Dysspondyloenchondromatosis (Orphanet:85198)
Fabry disease (Orphanet:324)
Fucosidosis (Orphanet:349)
Immunoglobulin A vasculitis (Orphanet:761)
Maffucci syndrome (Orphanet:163634)
Moyamoya disease (Orphanet:2573)
Mucocutaneous venous malformations (Orphanet:2451)
Parkes Weber syndrome (Orphanet:90307)
Proteus syndrome (Orphanet:744)
Scleroderma (Orphanet:801)
Sialidosis type 1 (Orphanet:812)
Sneddon syndrome (Orphanet:820)
Tufted angioma (Orphanet:1063)
Von Hippel-Lindau disease (Orphanet:892)