Conjunctival telangiectasia

Symptom Information:

Symptom ID: HPO:0000524
Synonyms:
Conjunctival telangiectases [HPO:0000524]
Telangiectasia, conjunctival [HPO:0000524]
Conjunctival telangiectasis (disorder) [Orphanet:4680]
Conjunctival telangiectasis [Orphanet:4680]
Conjunctival telangiectases [OMIM:Conjunctival telangiectases]
Conjunctival telangiectasia [OMIM:Conjunctival telangiectasia]
Telangiectasia, conjunctival [OMIM:Telangiectasia, conjunctival]
Conjunctival telangiectasia [Orphanet:4680]
Conjunctival telangiectasia (reported in 1 family) [OMIM:Conjunctival telangiectasia (reported in 1 family)]
Conjunctival telangiectasia [MedDRA:10072143]
Quality:
Cross references:
Orphanet:4680 "Conjunctival telangiectasia" [Orphanet:4680]
OMIM: "Conjunctival telangiectases" [OMIM:Conjunctival telangiectases]
OMIM: "Conjunctival telangiectasia" [OMIM:Conjunctival telangiectasia]
OMIM: "Telangiectasia, conjunctival" [OMIM:Telangiectasia, conjunctival]
OMIM: "Conjunctival telangiectasia (reported in 1 family)" [OMIM:Conjunctival telangiectasia (reported in 1 family)]
UMLS:C0239105 "Conjunctival telangiectasis" [Orphanet:4680]
Is a (Direct Parents):
HPO         Mucosal telangiectasiae
MedDRA Ocular vascular disorders NEC
Orphanet Abnormality of the eye
HPO         Abnormality of the vasculature of the conjunctiva
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the eye(HPO:0000478)
          Abnormal eye morphology(HPO:0012372)
             Abnormality of the globe(HPO:0012374)
                Abnormality of the vasculature of the eye(HPO:0008047)
                   Abnormality of the vasculature of the conjunctiva(HPO:0008054)
                      Conjunctival telangiectasia(HPO:0000524)
             Abnormality of the conjunctiva(HPO:0000502)
                Abnormality of the vasculature of the conjunctiva(HPO:0008054)
                   Conjunctival telangiectasia(HPO:0000524)
       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)
                      Mucosal telangiectasiae(HPO:0100579)
                         Conjunctival telangiectasia(HPO:0000524)
       Abnormality of the cardiovascular system(HPO:0001626)
          Abnormality of the vasculature(HPO:0002597)
             Abnormality of the vasculature of the eye(HPO:0008047)
                Abnormality of the vasculature of the conjunctiva(HPO:0008054)
                   Conjunctival telangiectasia(HPO:0000524)
MedDRA:
Vascular disorders(MedDRA:10047065)
    Vascular disorders NEC(MedDRA:10047066)
       Ocular vascular disorders NEC(MedDRA:10030067)
          Conjunctival telangiectasia(HPO:0000524)
Database Frequency: 17 / 7739
Resource:

All diseases associated with this symptom:

3MC SYNDROME 1 (OMIM:257920)
ATAXIA-TELANGIECTASIA WITH GENERALIZED SKIN PIGMENTATION AND EARLYDEATH (OMIM:208910)
ATAXIA-TELANGIECTASIA-LIKE DISORDER 2 (OMIM:615919)
Ataxia-telangiectasia (Orphanet:100)
EPILEPSY-TELANGIECTASIA (OMIM:226850)
Epilepsy telangiectasia (Orphanet:1951)
Fabry disease (Orphanet:324)
Galactosialidosis (Orphanet:351)
Hereditary hemorrhagic telangiectasia (Orphanet:774)
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 1 (OMIM:606002)
Spinocerebellar ataxia with axonal neuropathy type 2 (Orphanet:64753)
Sturge-Weber syndrome (Orphanet:3205)
TELANGIECTASIA, HEREDITARY HEMORRHAGIC, OF RENDU, OSLER, AND WEBER (OMIM:187300)
TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 2 (OMIM:600376)
TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 4 (OMIM:610655)
TRYPTOPHANURIA WITH DWARFISM (OMIM:276100)
Xeroderma pigmentosum (Orphanet:910)