Q92.8
ICD-10-CMThis code signifies the presence of an extra copy of a portion of an autosome, or an entire extra autosome, that is not specifically classified elsewhere. These genetic conditions result from an abnormal number of chromosomes, leading to a range of developmental and physical anomalies depending on the specific chromosome(s) involved and the extent of the duplication.
Assign this code when documentation confirms a trisomy or partial trisomy of an autosome that does not have a more specific ICD-10-CM code. This typically applies to rare or newly identified chromosomal abnormalities. Supporting documentation includes genetic testing results (e.g., karyotype, FISH, microarray) and clinical geneticist reports detailing the specific chromosomal aberration.
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