Telangiectasia
Symptom Information:
Symptom ID: | HPO:0001009 | |||||||||||||
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) Telangiectasia(HPO:0001009) MedDRA: Vascular disorders(MedDRA:10047065) Vascular disorders NEC(MedDRA:10047066) Vascular malformations and acquired anomalies(MedDRA:10047091) Telangiectasia(HPO:0001009) |
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Database Frequency: | 46 / 7739 | |||||||||||||
Resource: |
All diseases associated with this symptom:
ATAXIA-TELANGIECTASIA | (OMIM:208900) |
Ataxia-telangiectasia-like disorder | (Orphanet:251347) |
Bloom syndrome | (Orphanet:125) |
CEREBRAL CAVERNOUS MALFORMATIONS 2 | (OMIM:603284) |
CREST syndrome | (Orphanet:90290) |
Cerebroretinal vasculopathy | (Orphanet:3421) |
Cushing disease | (Orphanet:96253) |
Cushing syndrome | (Orphanet:553) |
Cutis marmorata telangiectatica congenita | (Orphanet:1556) |
DE SANCTIS-CACCHIONE SYNDROME | (OMIM:278800) |
DPM1-CDG | (Orphanet:79322) |
Deafness - intellectual deficit, Martin-Probst type | (Orphanet:85321) |
Familial cutaneous telangiectasia and oropharyngeal predisposition cancer syndrome | (Orphanet:313846) |
Focal dermal hypoplasia | (Orphanet:2092) |
Fucosidosis | (Orphanet:349) |
HERNS syndrome | (Orphanet:63261) |
Hallermann-Streiff syndrome | (Orphanet:2108) |
Hemochromatosis, type 1 | (OMIM:235200) |
Hemochromatosis, type 2A | (OMIM:602390) |
Hereditary vascular retinopathy | (Orphanet:71291) |
Hypotrichosis - lymphedema - telangiectasia | (Orphanet:69735) |
Idiopathic and/or familial pulmonary arterial hypertension | (Orphanet:422) |
JUVENILE POLYPOSIS/HEREDITARY HEMORRHAGIC TELANGIECTASIA SYNDROME | (OMIM:175050) |
Leber hereditary optic neuropathy | (Orphanet:104) |
Leber plus disease | (Orphanet:99718) |
Mandibular hypoplasia-deafness-progeroid syndrome | (Orphanet:363649) |
Moyamoya disease | (Orphanet:2573) |
Ramon syndrome | (Orphanet:3019) |
Retinal vasculopathy and cerebral leukodystrophy | (Orphanet:247691) |
Rothmund-Thomson syndrome | (Orphanet:2909) |
STING-ASSOCIATED VASCULOPATHY, INFANTILE-ONSET | (OMIM:615934) |
TELANGIECTASIA, HEREDITARY HEMORRHAGIC, OF RENDU, OSLER, AND WEBER | (OMIM:187300) |
TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 2 | (OMIM:600376) |
TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 4 | (OMIM:610655) |
TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 5 | (OMIM:615506) |
Transaldolase deficiency | (Orphanet:101028) |
UV-SENSITIVE SYNDROME 1 | (OMIM:600630) |
UV-SENSITIVE SYNDROME 3 | (OMIM:614640) |
UV-sensitive syndrome | (Orphanet:178338) |
Werner syndrome | (Orphanet:902) |
Xeroderma pigmentosum complementation group A | (Orphanet:276249) |
Xeroderma pigmentosum complementation group C | (Orphanet:276255) |
Xeroderma pigmentosum complementation group D | (Orphanet:276258) |
Xeroderma pigmentosum complementation group E | (Orphanet:276261) |
Xeroderma pigmentosum variant | (Orphanet:90342) |
Xeroderma pigmentosum/Cockayne syndrome complex | (Orphanet:220295) |