Telangiectasia of the skin

Symptom Information:

Symptom ID: HPO:0100585
Synonyms:
Skin telangiectasia [Orphanet:23630]
Telangiectasiae of the skin [Orphanet:23630]
Quality:
Cross references:
HPO:0001009 "Telangiectasia" [Orphanet:23630]
Orphanet:23630 "Telangiectasiae of the skin" [Orphanet:23630]
Is a (Direct Parents):
HPO         Telangiectasia
Orphanet Vascular skin abnormality
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)
                   Telangiectasia(HPO:0001009)
                      Telangiectasia of the skin(HPO:0100585)
MedDRA:
Database Frequency: 66 / 7739
Resource:

All diseases associated with this symptom:

1p36 deletion syndrome (Orphanet:1606)
Acrogeria (Orphanet:2500)
Adiposis dolorosa (Orphanet:36397)
Aggressive systemic mastocytosis (Orphanet:98850)
Alagille syndrome (Orphanet:52)
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)
Antisynthetase syndrome (Orphanet:81)
Arterial tortuosity syndrome (Orphanet:3342)
Ataxia-telangiectasia (Orphanet:100)
Bannayan-Riley-Ruvalcaba syndrome (Orphanet:109)
Bloom syndrome (Orphanet:125)
CREST syndrome (Orphanet:90290)
Cerebroretinal vasculopathy (Orphanet:3421)
Cockayne syndrome (Orphanet:191)
Cushing disease (Orphanet:96253)
Cushing syndrome (Orphanet:553)
Cutaneous lupus erythematosus (Orphanet:535)
Cutaneous mastocytosis (Orphanet:66646)
Cutis marmorata telangiectatica congenita (Orphanet:1556)
Deafness - intellectual deficit, Martin-Probst type (Orphanet:85321)
Dermatomyositis (Orphanet:221)
Diffuse cutaneous systemic sclerosis (Orphanet:220393)
Dyskeratosis congenita (Orphanet:1775)
Ehlers-Danlos syndrome, vascular type (Orphanet:286)
Epidermodysplasia verruciformis (Orphanet:302)
Fabry disease (Orphanet:324)
Familial cylindromatosis (Orphanet:211)
Familial multiple trichoepithelioma (Orphanet:867)
Focal dermal hypoplasia (Orphanet:2092)
HERNS syndrome (Orphanet:63261)
Hemochromatosis, type 1 (OMIM:235200)
Hereditary acrokeratotic poikiloderma, Weary type (Orphanet:2907)
Hereditary hemorrhagic telangiectasia (Orphanet:774)
Hereditary vascular retinopathy (Orphanet:71291)
Hypotrichosis - lymphedema - telangiectasia (Orphanet:69735)
Incontinentia pigmenti (Orphanet:464)
Juvenile dermatomyositis (Orphanet:93672)
Juvenile polyposis syndrome (Orphanet:2929)
LIG4 syndrome (Orphanet:99812)
Limited cutaneous systemic sclerosis (Orphanet:220402)
Limited systemic sclerosis (Orphanet:220407)
Maculopapular cutaneous mastocytosis (Orphanet:79457)
Malignant atrophic papulosis (Orphanet:679)
Marfanoid habitus - intellectual deficit, autosomal recessive (Orphanet:2463)
Mastocytosis (Orphanet:98292)
Megalencephaly-capillary malformation-polymicrogyria syndrome (Orphanet:60040)
Odonto-onycho-dermal dysplasia (Orphanet:2721)
Parkes Weber syndrome (Orphanet:90307)
Pediatric systemic sclerosis (Orphanet:93567)
Pseudoxanthoma elasticum (Orphanet:758)
Ramon syndrome (Orphanet:3019)
Retinal ischemic syndrome - digestive tract small vessel hyalinosis - diffuse cerebral calcifications (Orphanet:3018)
Retinal vasculopathy and cerebral leukodystrophy (Orphanet:247691)
Reynolds syndrome (Orphanet:779)
Rombo syndrome (Orphanet:3110)
Scleroderma (Orphanet:801)
Sternal malformation - vascular dysplasia (Orphanet:3195)
Systemic sclerosis (Orphanet:90291)
Transaldolase deficiency (Orphanet:101028)
Von Hippel-Lindau disease (Orphanet:892)
Werner syndrome (Orphanet:902)
Xeroderma pigmentosum (Orphanet:910)
Xeroderma pigmentosum variant (Orphanet:90342)