Other specified chromosome abnormalities. Q99.8 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. The 2021 edition of ICD-10-CM Q99.8 became effective on October 1, 2020.
ICD-9-CM 758.9 is a billable medical code that can be used to indicate a diagnosis on a reimbursement claim, however, 758.9 should only be used for claims with a date of service on or before September 30, 2015.
Q99.9 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. The 2018/2019 edition of ICD-10-CM Q99.9 became effective on October 1, 2018. This is the American ICD-10-CM version of Q99.9 - other international versions of ICD-10 Q99.9 may differ.
Other specified chromosome abnormalities 1 Autosomal aneuploidy. 2 Unbalanced chromosomal translocation (abnormal structure of chromosomes). 3 Unbalanced translocation of chromosome. 4 Undervirilization of male due to steroidogenic acute regulatory protein deficiency. 5 Undervirilized xy, star protein deficiency. 6 ... (more items)
ICD-10 Code for Encounter for other screening for genetic and chromosomal anomalies- Z13. 79- Codify by AAPC.
Q90. 0 (Down syndrome, Trisomy 21, nonmosaicism)
ICD-10 code F80. 89 for Other developmental disorders of speech and language is a medical classification as listed by WHO under the range - Mental, Behavioral and Neurodevelopmental disorders .
Down syndrome is a genetic disorder that results in an extra copy of chromosome 21. People with mosaic Down syndrome have a mixture of cells. Some have two copies of chromosome 21, and some have three. Mosaic Down syndrome occurs in about 2 percent of all Down syndrome cases.
Neuromuscular Re-education: 97112.
Down syndrome is a genetic disorder. It is also called trisomy 21. It includes certain birth defects, learning problems, and facial features.
Translocation Down syndrome refers to the type of Down syndrome that is caused by rearranged chromosome material. In this case, there are three # 21 chromosomes, just like there are in trisomy 21, but one of the 21 chromosomes is attached to another chromosome, instead of being separate.
315.9 - Unspecified delay in development. ICD-10-CM.