Syndromic genetic deafness

ICD-11 code : LD2H;

Preferred Label : Syndromic genetic deafness;

ICD-11 "other" category code : LD2H.Y;

ICD-11 "unspecified" category code : LD2H.Z;

Détails

Origin ID

186534168;

Automatic exact mappings (from CISMeF team)
- Congenital anomaly, other specified or unknown [ICPC-3 diagnosis]
Currated CISMeF NLP mapping
- Syndromic genetic deafness [ORDO Disease]
ICD-10 Mapping
- Other specified congenital malformation syndromes, not elsewhere classified [ICD-10 Sub-category]
Validated automatic mappings to NTBT
- Congenital disease (disorder) [SNOMED CT concept]
- Other specified congenital malformation syndromes, not elsewhere classified [ICD-10 Sub-category]

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

Vous pouvez consulter :

All resources
or only the major
or use the search engine

recommendations
documents concerning education
documents for patients