Congenital nuclear cataract
Symptom Information:
Symptom ID: | HPO:0008024 | ||||
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) Congenital cataract(HPO:0000519) Congenital nuclear cataract(HPO:0008024) Zonular cataract(HPO:0010920) Nuclear cataract(HPO:0100018) Congenital nuclear cataract(HPO:0008024) MedDRA: |
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Database Frequency: | 5 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
CATARACT 2, MULTIPLE TYPES | (OMIM:604307) |
CATARACT 40 | (OMIM:302200) |
CATARACT 41 | (OMIM:116400) |
Hereditary hyperferritinemia with congenital cataracts | (Orphanet:163) |
Tricho-oculo-dermo-vertebral syndrome | (Orphanet:3354) |