Nuclear cataract
Symptom Information:
Symptom ID: | HPO:0100018 | |||||
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) Zonular cataract(HPO:0010920) Nuclear cataract(HPO:0100018) MedDRA: Eye disorders(MedDRA:10015919) Anterior eye structural change, deposit and degeneration(MedDRA:10002693) Cataract conditions(MedDRA:10007772) Nuclear cataract(HPO:0100018) |
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Database Frequency: | 14 / 7739 | |||||
Resource: |
All diseases associated with this symptom:
CATARACT 1, MULTIPLE TYPES | (OMIM:116200) |
CATARACT 16, MULTIPLE TYPES | (OMIM:613763) |
CATARACT 17, MULTIPLE TYPES | (OMIM:611544) |
CATARACT 2, MULTIPLE TYPES | (OMIM:604307) |
CATARACT 22, MULTIPLE TYPES | (OMIM:609741) |
CATARACT 41 | (OMIM:116400) |
CATARACT 5, MULTIPLE TYPES | (OMIM:116800) |
CATARACT 9, MULTIPLE TYPES | (OMIM:604219) |
CATARACT, AGE-RELATED NUCLEAR | (OMIM:601371) |
Cataract-microcornea syndrome | (Orphanet:1377) |
Congenital cataract, Volkmann type | (Orphanet:98983) |
Dwarfism - intellectual deficit - eye abnormality | (Orphanet:2650) |
EXFOLIATION SYNDROME | (OMIM:177650) |
TRICHORRHEXIS NODOSA SYNDROME | (OMIM:275550) |