Telangiectasia

Symptom Information:

Symptom ID: HPO:0001009
Synonyms:
Cutaneous telangiectasia [HPO:0001009]
Telangiectases [HPO:0001009]
Skin telangiectasia [Orphanet:23630]
Cutaneous telangiectasia [OMIM:Cutaneous telangiectasia]
Telangiectases [OMIM:Telangiectases]
Telangiectasia [OMIM:Telangiectasia]
Telangiectasiae of the skin [Orphanet:23630]
Telangiectases (especially on tongue, lips, palate, face, conjunctiva, trunk, nail beds, fingers, and finger pads) [OMIM:Telangiectases (especially on tongue, lips, palate, face, conjunctiva, trunk, nail beds, fingers, and finger pads)]
Telangiectases (especially on tongue, lips, palate, fingers, face, conjunctiva, trunk, nail beds, and fingertips) [OMIM:Telangiectases (especially on tongue, lips, palate, fingers, face, conjunctiva, trunk, nail beds, and fingertips)]
Telangiectases (palms, soles, scalp, scrotum, legs) [OMIM:Telangiectases (palms, soles, scalp, scrotum, legs)]
Telangiectases (stomach, duodenum, small bowel, colon) [OMIM:Telangiectases (stomach, duodenum, small bowel, colon)]
Telangiectasia (soles) [OMIM:Telangiectasia (soles)]
Telangiectasia [MedDRA:10043189]
Quality:
Cross references:
HPO:0100585 "Teleangiectasia of the skin" [Orphanet:23630]
Orphanet:23630 "Telangiectasiae of the skin" [Orphanet:23630]
OMIM: "Cutaneous telangiectasia" [OMIM:Cutaneous telangiectasia]
OMIM: "Telangiectases" [OMIM:Telangiectases]
OMIM: "Telangiectasia" [OMIM:Telangiectasia]
OMIM: "Telangiectases (especially on tongue, lips, palate, face, conjunctiva, trunk, nail beds, fingers, and finger pads)" [OMIM:Telangiectases (especially on tongue, lips, palate, face, conjunctiva, trunk, nail beds, fingers, and finger pads)]
OMIM: "Telangiectases (especially on tongue, lips, palate, fingers, face, conjunctiva, trunk, nail beds, and fingertips)" [OMIM:Telangiectases (especially on tongue, lips, palate, fingers, face, conjunctiva, trunk, nail beds, and fingertips)]
OMIM: "Telangiectases (palms, soles, scalp, scrotum, legs)" [OMIM:Telangiectases (palms, soles, scalp, scrotum, legs)]
OMIM: "Telangiectases (stomach, duodenum, small bowel, colon)" [OMIM:Telangiectases (stomach, duodenum, small bowel, colon)]
OMIM: "Telangiectasia (soles)" [OMIM:Telangiectasia (soles)]
UMLS:C1963248 "Telangiectasia" [HPO:0001009]
Is a (Direct Parents):
Orphanet Vascular skin abnormality
HPO         Vascular skin abnormality
MedDRA Vascular malformations and acquired anomalies
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)
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)