Retinal fold
Symptom Information:
Symptom ID: | HPO:0008052 | ||
Synonyms: |
|
||
Quality: | |||
Cross references: |
|
||
Is a (Direct Parents): |
|
||
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 fold(HPO:0008052) MedDRA: |
||
Database Frequency: | 4 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Autosomal recessive chorioretinopathy-microcephaly | (Orphanet:2518) |
Congenital blindness due to retinal non-attachment | (Orphanet:300337) |
EXUDATIVE VITREORETINOPATHY 3 | (OMIM:605750) |
Norrie disease | (Orphanet:649) |