Chorioretinal degeneration

Symptom Information:

Symptom ID: HPO:0200065
Synonyms:
Choroidoretinal degeneration [OMIM:Choroidoretinal degeneration]
Choroidoretinal degeneration (1 patient) [OMIM:Choroidoretinal degeneration (1 patient)]
Choroidoretinal degeneration (starting in the midperiphery of the fundus and progressing centrally and peripherally) [OMIM:Choroidoretinal degeneration (starting in the midperiphery of the fundus and progressing centrally and peripherally)]
Quality:
Cross references:
OMIM: "Choroidoretinal degeneration" [OMIM:Choroidoretinal degeneration]
OMIM: "Choroidoretinal degeneration (1 patient)" [OMIM:Choroidoretinal degeneration (1 patient)]
OMIM: "Choroidoretinal degeneration (starting in the midperiphery of the fundus and progressing centrally and peripherally)" [OMIM:Choroidoretinal degeneration (starting in the midperiphery of the fundus and progressing centrally and peripherally)]
Is a (Direct Parents):
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)
                         Chorioretinal degeneration(HPO:0200065)
                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 degeneration(HPO:0200065)
                      Abnormality of the choroid(HPO:0000610)
                         Chorioretinal abnormality(HPO:0000532)
                            Chorioretinal degeneration(HPO:0200065)
MedDRA:
Database Frequency: 7 / 7739
Resource:

All diseases associated with this symptom:

Cholestasis - pigmentary retinopathy - cleft palate (Orphanet:1415)
Choroideremia (Orphanet:180)
Choroideremia - deafness - obesity (Orphanet:1435)
MENTAL RETARDATION, AUTOSOMAL DOMINANT 33 (OMIM:616311)
OPHTHALMOPLEGIA, EXTERNAL, AND MYOPIA (OMIM:311000)
RETINITIS PIGMENTOSA 2 (OMIM:312600)
RETINITIS PIGMENTOSA 6 (OMIM:312612)