Cataract, age-related nuclear

Preferred Label : Cataract, age-related nuclear;

Type : Other, mainly phenotypes with suspected mendelian basis;

Alternative titles and symbols : Nuclear sclerosis of the lens;

Inheritance : Autosomal recessive gene accounts for 35% of variability;

Prefixed ID : 601371;

Details

Origin ID

601371;

UMLS CUI

C1832423;

Automatic exact mappings (from CISMeF team)
- Early-onset non-syndromic cataract [ORDO Disease]
- Early-onset nuclear cataract [ORDO Disease]
Currated CISMeF NLP mapping
- Age-related nuclear cataract [ICD-10 Sub-category]
- Age-related nuclear cataract [HPO term]
- Nuclear age-related cataract [ICD-11 More detail]
- Nuclear senile cataract (disorder) [SNOMED CT concept]
- Senile nuclear sclerosis [MedDRA LLT]
- cataract, Age-Related nuclear [MeSH concept]
- cataract, Age-Related nuclear [MeSH Supplementary Concept]
- nuclear senile cataract [DO Concept]
- nuclear senile cataract [Disease (Nov.)]
- senile nuclear cataract [SNOMED Notion]
DO Cross reference
- cataract [DO Concept]
HPO term(s)
- Autosomal recessive inheritance [HPO term]
- Nuclear cataract [HPO term]
Semantic type(s)
- Pathologic Function [UMLS semantic type]
UMLS correspondences (same concept)
- Age-related nuclear cataract [ICD-10 Sub-category]
- Age-related nuclear cataract [HPO term]
- cataract, Age-Related nuclear [MeSH Supplementary Concept]
- cataract, Age-Related nuclear [MeSH concept]

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