Aniridia - CISMeF

ICD-11 code : LA11.3;

Preferred Label : Aniridia;

ICD-11 definition : Aniridia is a congenital ocular malformation characterized by the complete or partial absence of the iris. It can be isolated or part of a syndrome (isolated and syndromic aniridia; see these terms).;

ICD-11 synonym : congenital absence of iris; irideremia; hereditary aniridia; aplasia of iris; agenesis of iris; congenital aniridia; absent iris; sporadic aniridia; Absence of iris;

Details

Origin ID

970699895;

UMLS CUI

C0003076;

Automatic exact mappings (from CISMeF team)
- Aniridia [ICD-9 code]
- Aniridia [OMIM phenotypic series]
- paired box 6 [HGNC gene]
Currated CISMeF NLP mapping
- ANIRIDIA [WHO-ART Included Term]
- Absence of iris [ICD-10 Sub-category]
- Aniridia [PASCAL descriptor]
- Aniridia [NCIt concept]
- Aniridia [MedDRA Preferred Term]
- Aniridia [ORDO Disease]
- Aniridia [HPO term]
- Congenital aniridia (disorder) [SNOMED CT concept]
- aniridia [SNOMED Notion]
- aniridia [MeSH Descriptor]
- aniridia [DO Concept]
- aniridia [MeSH concept]
ICD-10 Mapping
- Absence of iris [ICD-10 Sub-category]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
UMLS correspondences (same concept)
- ANIRIDIA [WHO-ART Included Term]
- Absence of iris [ICD-10 Sub-category]
- Aniridia [ICD-9 code]
- Aniridia [HPO term]
- Aniridia [MedDRA Preferred Term]
- Aniridia [NCIt concept]
- Aniridia [ORDO Disease]
- Aniridia 1 [OMIM Phenotype]
- Congenital aniridia (disorder) [SNOMED CT concept]
- Isolated aniridia [ORDO Disease]
- aniridia [DO Concept]
- aniridia [MeSH Descriptor]
- aniridia [MeSH concept]
- aniridia [Disease (Nov.)]
- aniridia [SNOMED Notion]
- congenital aniridia [Disease (Nov.)]

Keyword's position in hierarchy(ies) :

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