Retinoblastoma

ICD-11 code : 2D02.2;

Preferred Label : Retinoblastoma;

ICD-11 definition : Retinoblastoma is the most common intraocular malignancy in children. It is a life threatening condition but is potentially curable. It can be hereditary or non-hereditary, unilateral or bilateral (unilateral retinoblastoma, bilateral retinoblastoma, see these terms).;

Détails

Origin ID

1855353671;

Automatic exact mappings (from CISMeF team)
- NCI CTEP SDC Retinoblastoma Sub-Category Terminology [NCIt concept]
- Neoplasm of eye or adnexa [ICPC-3 diagnosis]
- eye cancer [MedlinePlus Topic]
Currated CISMeF NLP mapping
- RETINOBLASTOMA [WHO-ART Preferred Term]
- Retinoblastoma [HPO term]
- Retinoblastoma [NCIt concept]
- Retinoblastoma [MedDRA Preferred Term]
- Retinoblastoma [OMIM Phenotype]
- Retinoblastoma [HRDO Sign]
- Retinoblastoma [PASCAL descriptor]
- Retinoblastoma [ORDO Disease]
- Retinoblastoma (disorder) [SNOMED CT concept]
- Retinoblastoma (morphologic abnormality) [SNOMED CT concept]
- retinoblastoma [MeSH Descriptor]
- retinoblastoma [MeSH concept]
- retinoblastoma [DO Concept]
- retinoblastoma [Radlex concept]
- retinoblastoma, nos [SNOMED Notion]
ICD-10 Mapping
- Malignant neoplasm of retina [ICD-10 Sub-category]
Validated automatic mappings to NTBT
- Malignant neoplasm of retina [ICD-10 Sub-category]

Position du mot-clé dans l'(les) arborescence(s) :

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