Posterior subcapsular cataract
Symptom Information:
Symptom ID: | HPO:0007787 | |||||||||
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 anterior segment of the globe(HPO:0004328) Abnormality of the lens(HPO:0000517) Cataract(HPO:0000518) Polar cataract(HPO:0010696) Subcapsular cataract(HPO:0000523) Posterior subcapsular cataract(HPO:0007787) MedDRA: |
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Database Frequency: | 20 / 7739 | |||||||||
Resource: |
All diseases associated with this symptom:
Alström syndrome | (Orphanet:64) |
Bardet-Biedl syndrome 1 | (OMIM:209900 ) |
Bardet-Biedl syndrome 10 | (OMIM:615987) |
Bardet-Biedl syndrome 2 | (OMIM:615981) |
Bardet-Biedl syndrome 5 | (OMIM:615983) |
Bardet-Biedl syndrome 7 | (OMIM:615984) |
CATARACT 31, MULTIPLE TYPES | (OMIM:605387) |
CATARACT 9, MULTIPLE TYPES | (OMIM:604219) |
CATARACT, ATAXIA, SHORT STATURE, AND MENTAL RETARDATION | (OMIM:300619) |
DEAFNESS, CATARACT, RETINITIS PIGMENTOSA, AND SPERM ABNORMALITIES | (OMIM:300719) |
Gyrate atrophy of choroid and retina | (Orphanet:414) |
KYRLE DISEASE | (OMIM:149500) |
MELAS | (Orphanet:550) |
Microcornea-myopic chorioretinal atrophy-telecanthus syndrome | (Orphanet:369970) |
RETINITIS PIGMENTOSA 23 | (OMIM:300424) |
RETINITIS PIGMENTOSA 27 | (OMIM:613750) |
RETINITIS PIGMENTOSA 56 | (OMIM:613581) |
RETINITIS PIGMENTOSA 66 | (OMIM:615233) |
RUIJS-AALFS SYNDROME | (OMIM:616200) |
SPONASTRIME dysplasia | (Orphanet:93357) |