Subcapsular cataract
Symptom Information:
Symptom ID: | HPO:0000523 | ||||||||
Synonyms: |
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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) MedDRA: Eye disorders(MedDRA:10015919) Anterior eye structural change, deposit and degeneration(MedDRA:10002693) Cataract conditions(MedDRA:10007772) Subcapsular cataract(HPO:0000523) |
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Database Frequency: | 12 / 7739 | ||||||||
Resource: |
All diseases associated with this symptom:
Alström syndrome | (Orphanet:64) |
Autosomal recessive spastic paraplegia type 48 | (Orphanet:306511) |
CATARACT 43 | (OMIM:616279) |
CUTIS VERTICIS GYRATA, RETINITIS PIGMENTOSA, AND SENSORINEURAL DEAFNESS | (OMIM:605685) |
Dorfman-Chanarin disease | (Orphanet:98907) |
ECTODERMAL DYSPLASIA WITH MENTAL RETARDATION AND SYNDACTYLY | (OMIM:600906) |
ENAMEL HYPOPLASIA, CATARACTS, AND AQUEDUCTAL STENOSIS | (OMIM:600907) |
EXUDATIVE VITREORETINOPATHY 4 | (OMIM:601813) |
Familial exudative vitreoretinopathy | (Orphanet:891) |
Polyneuropathy - hearing loss - ataxia - retinitis pigmentosa - cataract | (Orphanet:171848) |
Retinitis pigmentosa - intellectual deficit - deafness - hypogenitalism | (Orphanet:3085) |
Retinopathy of prematurity | (Orphanet:90050) |