Congenital malformation of inner ear

Preferred Label : Congenital malformation of inner ear;

Inclusion CIM-10 : Congenital anomaly of membranous labyrinth; Congenital anomaly of organ of Corti;

Diag associé à un acte (%) : 100.0;

Source : OMS;

Date de début : 01/01/1997;

Details

Origin ID

Q165;

UMLS CUI

C0685874;

Automatic exact mappings (from CISMeF team)
- Congenital anomaly of membranous labyrinth (disorder) [SNOMED CT concept]
- Congenital anomaly of organ of Corti (disorder) [SNOMED CT concept]
Currated CISMeF NLP mapping
- Anomalies of inner ear [ICD-9 code]
- Anomaly of inner ear congenital NOS [MedDRA LLT]
- Congenital abnormal shape of inner ear (disorder) [SNOMED CT concept]
- Congenital anomaly of inner ear [MedDRA Preferred Term]
- Congenital anomaly of inner ear (disorder) [SNOMED CT concept]
- Structural developmental anomalies of inner ear [ICD-11 Subcategory]
- congenital abnormal shape of inner ear [SNOMED Notion]
- congenital anomaly of inner ear [SNOMED Notion]
Orphanet concepts
- Cochleovestibular malformation [ORDO Disease]
- Deafness with labyrinthine aplasia, microtia, and microdontia [ORDO Disease]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
UMLS correspondences (same concept)
- Anomalies of inner ear [ICD-9 code]
- Anomaly of inner ear congenital NOS [MedDRA LLT]
- Congenital abnormal shape of inner ear (disorder) [SNOMED CT concept]
- Congenital anomaly of inner ear [MedDRA Preferred Term]
- Congenital anomaly of inner ear (disorder) [SNOMED CT concept]
- Structural developmental anomalies of inner ear [ICD-11 Subcategory]
- congenital abnormal shape of inner ear [SNOMED Notion]
- congenital anomaly of inner ear [SNOMED Notion]

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