Congenital ectropion

Preferred Label : Congenital ectropion;

Rare : true;

Diag associé à un acte (%) : 87.5;

Source : OMS;

Date de début : 01/01/1997;

Details

Origin ID

Q101;

UMLS CUI

C0266578;

Currated CISMeF NLP mapping
- Congenital ectropion [ORDO Disease]
- Congenital ectropion [ICD-11 Sub-sub category]
- Congenital ectropion (disorder) [SNOMED CT concept]
- congenital ectropion [SNOMED Notion]
Excluded by
- Other disorders of eyelid [ICD-10 category]
Manual NTBT mappings (CISMeF)
- Blepharo-cheilo-odontic syndrome [ORDO Disease]
- Euryblepharon [ORDO Disease]
- Isolated congenital ectropion [ORDO Disease]
Orphanet concepts
- Congenital ectropion [ORDO Disease]
- Euryblepharon [ORDO Disease]
- Isolated congenital ectropion [ORDO Disease]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
UMLS correspondences (same concept)
- Congenital ectropion [ORDO Disease]
- Congenital ectropion [ICD-11 Sub-sub category]
- Congenital ectropion (disorder) [SNOMED CT concept]
- congenital ectropion [SNOMED Notion]
Validated automatic mappings to BTNT
- Congenital ectropion uveae [ORDO Disease]

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