Abnormality of the retinal vasculature

Symptom Information:

Symptom ID: HPO:0008046
Synonyms:
Quality:
Cross references:
Is a (Direct Parents):
HPO         Retinal vascular tortuosity
HPO         Abnormality of the vasculature of the eye
HPO         Retinal neovascularization
HPO         Abnormality of the retina
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 retinal vasculature(HPO:0008046)
                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)
       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)
MedDRA:
Database Frequency: 41 / 7739
Resource:

All diseases associated with this symptom:

Angioma serpiginosum (Orphanet:95429)
Autosomal recessive cerebelloparenchymal disorder type 3 (Orphanet:1170)
CADASIL (Orphanet:136)
Cerebroretinal vasculopathy (Orphanet:3421)
Classic Bartter syndrome (Orphanet:93605)
Coats disease (Orphanet:190)
Cowden syndrome (Orphanet:201)
Ethylmalonic encephalopathy (Orphanet:51188)
Facioscapulohumeral dystrophy (Orphanet:269)
GM1 gangliosidosis (Orphanet:354)
Glutaryl-CoA dehydrogenase deficiency (Orphanet:25)
HEC syndrome (Orphanet:2119)
HERNS syndrome (Orphanet:63261)
Hereditary hemorrhagic telangiectasia (Orphanet:774)
Hereditary vascular retinopathy (Orphanet:71291)
Incontinentia pigmenti (Orphanet:464)
Microscopic polyangiitis (Orphanet:727)
Neurofibromatosis type 2 (Orphanet:637)
Neuronal ceroid lipofuscinosis (Orphanet:216)
Night blindness - skeletal anomalies - dysmorphism (Orphanet:1390)
Norrie disease (Orphanet:649)
Oculo-reno-cerebellar syndrome (Orphanet:2715)
PHACE syndrome (Orphanet:42775)
Polyarteritis nodosa (Orphanet:767)
Progressive bifocal chorioretinal atrophy (Orphanet:75373)
Retinal ischemic syndrome - digestive tract small vessel hyalinosis - diffuse cerebral calcifications (Orphanet:3018)
Retinal vasculopathy and cerebral leukodystrophy (Orphanet:247691)
Retinitis pigmentosa (Orphanet:791)
Retinopathy - anemia- central nervous system anomalies (Orphanet:3088)
Rift valley fever (Orphanet:319251)
Short stature - craniofacial anomalies - genital hypoplasia (Orphanet:2994)
Sneddon syndrome (Orphanet:820)
Sturge-Weber syndrome (Orphanet:3205)
Trisomy 13 (Orphanet:3378)
Von Hippel anomaly (Orphanet:98941)
Von Hippel-Lindau disease (Orphanet:892)
Waldenström macroglobulinemia (Orphanet:33226)
Williams syndrome (Orphanet:904)
Woolly hair (Orphanet:170)
Wyburn-Mason syndrome (Orphanet:53719)
X-linked retinal dysplasia (Orphanet:1852)