Congenital chorioretinal dystrophy

Symptom Information:

Symptom ID: HPO:0007920
Synonyms:
Congenital chorioretinal dystrophy [OMIM:Congenital chorioretinal dystrophy]
Quality:
Cross references:
OMIM: "Congenital chorioretinal dystrophy" [OMIM:Congenital chorioretinal dystrophy]
Is a (Direct Parents):
HPO         Chorioretinal dystrophy
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 choroid(HPO:0000610)
                         Chorioretinal abnormality(HPO:0000532)
                            Chorioretinal dystrophy(HPO:0001135)
                               Congenital chorioretinal dystrophy(HPO:0007920)
                      Abnormality of the retina(HPO:0000479)
                         Chorioretinal abnormality(HPO:0000532)
                            Chorioretinal dystrophy(HPO:0001135)
                               Congenital chorioretinal dystrophy(HPO:0007920)
                Abnormality of the uvea(HPO:0000553)
                   Abnormality of the choroid(HPO:0000610)
                      Chorioretinal abnormality(HPO:0000532)
                         Chorioretinal dystrophy(HPO:0001135)
                            Congenital chorioretinal dystrophy(HPO:0007920)
MedDRA:
Database Frequency: 1 / 7739
Resource:

All diseases associated with this symptom:

Progressive bifocal chorioretinal atrophy (Orphanet:75373)