Telangiectasia of the skin
Symptom Information:
Symptom ID: | HPO:0100585 | ||||
Synonyms: |
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Quality: | |||||
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) Telangiectasia(HPO:0001009) Telangiectasia of the skin(HPO:0100585) MedDRA: |
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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) |