Vitreoretinal degeneration
Symptom Information:
Symptom ID: | HPO:0000655 | ||
Synonyms: |
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Quality: | |||
Cross references: |
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Is a (Direct Parents): |
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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: |
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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) |