Cortical cataract
Symptom Information:
Symptom ID: | HPO:0100019 | ||||
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 anterior segment of the globe(HPO:0004328) Abnormality of the lens(HPO:0000517) Cataract(HPO:0000518) Zonular cataract(HPO:0010920) Cortical cataract(HPO:0100019) MedDRA: Eye disorders(MedDRA:10015919) Anterior eye structural change, deposit and degeneration(MedDRA:10002693) Cataract conditions(MedDRA:10007772) Cortical cataract(HPO:0100019) |
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Database Frequency: | 3 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
Autosomal recessive childhood-onset cortical cataract | (Orphanet:217046) |
CATARACT 9, MULTIPLE TYPES | (OMIM:604219) |
CUTIS VERTICIS GYRATA, RETINITIS PIGMENTOSA, AND SENSORINEURAL DEAFNESS | (OMIM:605685) |