Peripapillary chorioretinal atrophy

Symptom Information:

Symptom ID: HPO:0007950
Synonyms:
Peripapillary chorioretinal atrophy [OMIM:Peripapillary chorioretinal atrophy]
Quality:
Cross references:
OMIM: "Peripapillary chorioretinal atrophy" [OMIM:Peripapillary chorioretinal atrophy]
Is a (Direct Parents):
HPO         Chorioretinal atrophy
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 uvea(HPO:0000553)
                   Abnormality of the choroid(HPO:0000610)
                      Chorioretinal abnormality(HPO:0000532)
                         Chorioretinal atrophy(HPO:0000533)
                            Peripapillary chorioretinal atrophy(HPO:0007950)
                Abnormality of the posterior segment of the globe(HPO:0004329)
                   Abnormality of the fundus(HPO:0001098)
                      Abnormality of the retina(HPO:0000479)
                         Chorioretinal abnormality(HPO:0000532)
                            Chorioretinal atrophy(HPO:0000533)
                               Peripapillary chorioretinal atrophy(HPO:0007950)
                      Abnormality of the choroid(HPO:0000610)
                         Chorioretinal abnormality(HPO:0000532)
                            Chorioretinal atrophy(HPO:0000533)
                               Peripapillary chorioretinal atrophy(HPO:0007950)
MedDRA:
Database Frequency: 3 / 7739
Resource:

All diseases associated with this symptom:

Helicoid peripapillary chorioretinal degeneration (Orphanet:86813)
Pseudoxanthoma elasticum (Orphanet:758)
RETINITIS PIGMENTOSA 27 (OMIM:613750)