Retinal telangiectasia

Symptom Information:

Symptom ID: HPO:0007763
Synonyms:
Retinal telangiectasia (disorder) [Orphanet:5120]
Retinal vascular anomaly (finding) [Orphanet:5120]
Retinal telangiectasia [Orphanet:5120]
Retinal vascular anomaly [Orphanet:5120]
Retinal telangiectasia [OMIM:Retinal telangiectasia]
Retinal vascular anomalies/retinal telangiectasia [Orphanet:5120]
Retinal telangiectasia [MedDRA:10038899]
Parafoveal telangiectasia [MedDRA:10038899]
Quality:
Cross references:
Orphanet:5120 "Retinal vascular anomalies/retinal telangiectasia" [Orphanet:5120]
OMIM: "Retinal telangiectasia" [OMIM:Retinal telangiectasia]
UMLS:C0154835 "Retinal telangiectasia" [Orphanet:5120]
UMLS:C0423400 "Retinal vascular anomaly" [Orphanet:5120]
Is a (Direct Parents):
HPO         Abnormality of the retinal vasculature
HPO         Telangiectasia
Orphanet Abnormality of the eye
MedDRA Vascular malformations and acquired anomalies
HPO         Macular telangiectasia
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       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 retinal vasculature(HPO:0008046)
                   Retinal telangiectasia(HPO:0007763)
       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)
                      Retinal telangiectasia(HPO:0007763)
       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 retinal vasculature(HPO:0008046)
                      Retinal telangiectasia(HPO:0007763)
                Abnormality of the posterior segment of the globe(HPO:0004329)
                   Abnormality of the fundus(HPO:0001098)
                      Abnormality of the retina(HPO:0000479)
                         Abnormality of the retinal vasculature(HPO:0008046)
                            Retinal telangiectasia(HPO:0007763)
MedDRA:
Vascular disorders(MedDRA:10047065)
    Vascular disorders NEC(MedDRA:10047066)
       Vascular malformations and acquired anomalies(MedDRA:10047091)
          Retinal telangiectasia(HPO:0007763)
Database Frequency: 6 / 7739
Resource:

All diseases associated with this symptom:

CADASIL (Orphanet:136)
Cerebroretinal vasculopathy (Orphanet:3421)
Coats plus syndrome (Orphanet:313838)
Facioscapulohumeral dystrophy (Orphanet:269)
HERNS syndrome (Orphanet:63261)
RETINAL TELANGIECTASIA AND HYPOGAMMAGLOBULINEMIA (OMIM:267900)