Chorioretinopathy

Symptom Information:

Symptom ID: HPO:0001145
Synonyms:
Chorioretinopathy [OMIM:Chorioretinopathy]
Chorioretinopathy [MedDRA:10063118]
Quality:
Cross references:
OMIM: "Chorioretinopathy" [OMIM:Chorioretinopathy]
UMLS:C0339383 "Chorioretinopathy" [HPO:0001145]
Is a (Direct Parents):
MedDRA Choroid and vitreous structural change, deposit and degeneration
HPO         Chorioretinal abnormality
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)
                         Chorioretinopathy(HPO:0001145)
                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)
                            Chorioretinopathy(HPO:0001145)
                      Abnormality of the choroid(HPO:0000610)
                         Chorioretinal abnormality(HPO:0000532)
                            Chorioretinopathy(HPO:0001145)
MedDRA:
Eye disorders(MedDRA:10015919)
    Ocular structural change, deposit and degeneration NEC(MedDRA:10042261)
       Choroid and vitreous structural change, deposit and degeneration(MedDRA:10008776)
          Chorioretinopathy(HPO:0001145)
Database Frequency: 3 / 7739
Resource:

All diseases associated with this symptom:

Autosomal recessive chorioretinopathy-microcephaly (Orphanet:2518)
Chorioretinopathy, Birdshot type (Orphanet:179)
Microcephaly - lymphedema - chorioretinopathy (Orphanet:2526)