Subcapsular cataract

Symptom Information:

Symptom ID: HPO:0000523
Synonyms:
Subcapsular cataracts [HPO:0000523]
Subcapsular lenticular cataracts [HPO:0000523]
Subcapsular opacities [HPO:0000523]
Subcapsular cataract [OMIM:Subcapsular cataract]
Subcapsular cataracts [OMIM:Subcapsular cataracts]
Subcapsular lenticular cataracts [OMIM:Subcapsular lenticular cataracts]
Subcapsular opacities [OMIM:Subcapsular opacities]
Cataract subcapsular [MedDRA:10007764]
Quality:
Cross references:
OMIM: "Subcapsular cataract" [OMIM:Subcapsular cataract]
OMIM: "Subcapsular cataracts" [OMIM:Subcapsular cataracts]
OMIM: "Subcapsular lenticular cataracts" [OMIM:Subcapsular lenticular cataracts]
OMIM: "Subcapsular opacities" [OMIM:Subcapsular opacities]
Is a (Direct Parents):
HPO         Polar cataract
MedDRA Cataract conditions
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)
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)