Congenital aphakia

ICD-11 code : LA12.2;

Preferred Label : Congenital aphakia;

ICD-11 definition : Congenital primary aphakia is a developmental eye defect characterised by an absence of the lens, and can be associated with variable secondary ocular defects (including aplasia/dysplasia of the anterior segment of the eye, microphthalmia, and in some cases absence of the iris, retinal dysplasia, or sclerocornea).;

ICD-11 synonym : congenital absence of lens; agenesis of lens;

Details

Origin ID

885383581;

UMLS CUI

C0152422;

Automatic exact mappings (from CISMeF team)
- Congenital aphakia [HPO term]
Currated CISMeF NLP mapping
- Aphakia congenital [MedDRA Preferred Term]
- Congenital Aphakia [NCIt concept]
- Congenital aphakia [MedDRA LLT]
- Congenital aphakia [ICD-9 code]
- Congenital aphakia [PASCAL descriptor]
- Congenital aphakia [ICD-10 Sub-category]
- Congenital aphakia [ICD-10 Sub-category (who)]
- Congenital aphakia (disorder) [SNOMED CT concept]
- congenital aphakia [DO Concept]
- congenital aphakia [SNOMED Notion]
ICD-10 Mapping
- Congenital aphakia [ICD-10 Sub-category]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
UMLS correspondences (same concept)
- Aphakia congenital [MedDRA Preferred Term]
- Congenital Aphakia [NCIt concept]
- Congenital aphakia [ICD-9 code]
- Congenital aphakia [HPO term]
- Congenital aphakia [ICD-10 Sub-category]
- Congenital aphakia [MedDRA LLT]
- Congenital aphakia (disorder) [SNOMED CT concept]
- congenital aphakia [DO Concept]
- congenital aphakia [SNOMED Notion]
Validated automatic mappings to BTNT
- Congenital primary aphakia [ORDO Disease]

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