Falciform retinal fold

Symptom Information:

Symptom ID: HPO:0001493
Synonyms:
Congenital retinal fold [HPO:0001493]
Falciform retinal fold [OMIM:Falciform retinal fold]
Congenital retinal folds [OMIM:Congenital retinal folds]
Falciform retinal folds [OMIM:Falciform retinal folds]
Quality:
Cross references:
OMIM: "Falciform retinal fold" [OMIM:Falciform retinal fold]
OMIM: "Congenital retinal folds" [OMIM:Congenital retinal folds]
OMIM: "Falciform retinal folds" [OMIM:Falciform retinal folds]
Is a (Direct Parents):
HPO         Retinal fold
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)
                            Falciform retinal fold(HPO:0001493)
MedDRA:
Database Frequency: 6 / 7739
Resource:

All diseases associated with this symptom:

EXUDATIVE VITREORETINOPATHY 2, X-LINKED (OMIM:305390)
EXUDATIVE VITREORETINOPATHY 4 (OMIM:601813)
Familial exudative vitreoretinopathy (Orphanet:891)
RETINAL NONATTACHMENT AND FALCIFORM DETACHMENT (OMIM:180070)
Retinopathy of prematurity (Orphanet:90050)
X-linked retinal dysplasia (Orphanet:1852)