Retinal fold

Symptom Information:

Symptom ID: HPO:0008052
Synonyms:
Quality:
Cross references:
Is a (Direct Parents):
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 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)