LA55ICD-11 MMS 2026-01
Compression facies
Description
A disease caused by neurovascular compression of the facial nerve. This disease is characterised by facial spasm, and abnormal facial expression.
Index terms
- Compression facies
Exclusions from above levels
- http://id.who.int/icd/entity/733825440 – Inborn errors of metabolism
Sibling codes
LA30– Structural developmental anomalies of teeth and periodontal tissuesLA31– Structural developmental anomalies of mouth or tongueLA50– Congenital velopharyngeal incompetenceLA51– Facial cleftsLA52– Facial asymmetryLA53– MacrocheiliaLA54– MicrocheiliaLA56– Pierre Robin syndromeLA5Y– Other specified structural developmental anomalies of the faceLA5Z– Structural developmental anomalies of the face, unspecified
Foundation entity
Compression facies – http://id.who.int/icd/entity/1935903902
Part of: 20: Developmental anomalies