ICD-11 code : L2-LD5;
Preferred Label : Sex chromosome anomalies;
ICD-11 definition : Any disease caused by change in the number or structure of the X or Y chromosome.
Confirmation is by observation of a chromosomal anomaly by genetic testing.;
ICD-11 "other" category code : LD5Y;
ICD-11 "unspecified" category code : LD5Z;
Origin ID : 1703057973;
Currated CISMeF NLP mapping
Any disease caused by change in the number or structure of the X or Y chromosome.
Confirmation is by observation of a chromosomal anomaly by genetic testing.