ICD-9-CM Code 758.81 to ICD-10-CM
ICD-10 Equivalent of 758.81:
As of October 2015, ICD-9 codes are no longer used for medical coding. Instead, use the following eight equivalent ICD-10-CM codes, which are an approximate match to ICD-9 code 758.81:
- ICD-10 Code Q970, Karyotype 47, XXX (billable)
- ICD-10 Code Q971, Female with more than three X chromosomes (billable)
- ICD-10 Code Q972, Mosaicism, lines with various numbers of X chromosomes (billable)
- ICD-10 Code Q978, Other specified sex chromosome abnormalities, female phenotype (billable)
- ICD-10 Code Q985, Karyotype 47, XYY (billable)
- ICD-10 Code Q987, Male with sex chromosome mosaicism (billable)
- ICD-10 Code Q988, Other specified sex chromosome abnormalities, male phenotype (billable)
- ICD-10 Code Q998, Other specified chromosome abnormalities (billable)
Historical Information for ICD-9 Code 758.81
BILLABLE ICD-9 CODE
POA EXEMPT
Billable Code
Billable codes are sufficient justification for admission to an acute care hospital when used a principal diagnosis.Long ICD9 Description: Other conditions due to sex chromosome anomalies
Short ICD9 Description: Oth cond due to sex chrm
Parent Code: 758.8 - Other conditions due to chromosome anomalies