Retinal vascular malformation

Symptom Information:

Symptom ID: HPO:0007797
Synonyms:
Retinal vascular malformations [OMIM:Retinal vascular malformations]
Quality:
Cross references:
OMIM: "Retinal vascular malformations" [OMIM:Retinal vascular malformations]
Is a (Direct Parents):
HPO         Abnormality of the retinal vasculature
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 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 vascular malformation(HPO:0007797)
                Abnormality of the vasculature of the eye(HPO:0008047)
                   Abnormality of the retinal vasculature(HPO:0008046)
                      Retinal vascular malformation(HPO:0007797)
       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 vascular malformation(HPO:0007797)
MedDRA:
Database Frequency: 2 / 7739
Resource:

All diseases associated with this symptom:

CEREBRAL CAVERNOUS MALFORMATIONS (OMIM:116860)
Hereditary cerebral cavernous malformation (Orphanet:221061)