Chorioretinal abnormality
Symptom Information:
Symptom ID: | HPO:0000532 | ||||
Synonyms: |
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Is a (Direct Parents): |
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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) Abnormality of the retina(HPO:0000479) Chorioretinal abnormality(HPO:0000532) Abnormality of the uvea(HPO:0000553) Abnormality of the choroid(HPO:0000610) Chorioretinal abnormality(HPO:0000532) MedDRA: |
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Database Frequency: | 5 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
Alström syndrome | (Orphanet:64) |
Chorioretinopathy, Birdshot type | (Orphanet:179) |
LEUKOENCEPHALOPATHY WITH ATAXIA | (OMIM:615651) |
Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency | (Orphanet:5) |
Maternally-inherited diabetes and deafness | (Orphanet:225) |