Retinal pigment epithelial atrophy
Symptom Information:
Symptom ID: | HPO:0007722 | ||
Synonyms: |
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Quality: | |||
Cross references: |
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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 retina(HPO:0000479) obsolete Abnormality of the retinal pigment epithelium(HPO:0008051) Retinal pigment epithelial atrophy(HPO:0007722) MedDRA: |
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Database Frequency: | 10 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Alström syndrome | (Orphanet:64) |
Chorioretinopathy, Birdshot type | (Orphanet:179) |
Microphthalmia - retinitis pigmentosa - foveoschisis - optic disc drusen | (Orphanet:251279) |
RETINITIS PIGMENTOSA 19 | (OMIM:601718) |
RETINITIS PIGMENTOSA 31 | (OMIM:609923) |
RETINITIS PIGMENTOSA 33 | (OMIM:610359) |
RETINITIS PIGMENTOSA 44 | (OMIM:613769) |
Retinal macular dystrophy type 2 | (Orphanet:319640) |
Retinopathy, Burgess-Black type | (Orphanet:139455) |
Wagner disease | (Orphanet:898) |