Vitreoretinal degeneration

Symptom Information:

Symptom ID: HPO:0000655
Synonyms:
Vitreoretinal degeneration [OMIM:Vitreoretinal degeneration]
Quality:
Cross references:
OMIM: "Vitreoretinal degeneration" [OMIM:Vitreoretinal degeneration]
Is a (Direct Parents):
HPO         Retinal degeneration
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)
                         Retinal degeneration(HPO:0000546)
                            Vitreoretinal degeneration(HPO:0000655)
MedDRA:
Database Frequency: 8 / 7739
Resource:

All diseases associated with this symptom:

Goldmann-Favre syndrome (Orphanet:53540)
Knobloch syndrome (Orphanet:1571)
Marshall syndrome (Orphanet:560)
Pigmented paravenous retinochoroidal atrophy (Orphanet:251295)
STICKLER SYNDROME, TYPE V (OMIM:614284)
Snowflake vitreoretinal degeneration (Orphanet:91496)
Spondyloepiphyseal dysplasia congenita (Orphanet:94068)
Wagner disease (Orphanet:898)