| Diagnostic Grouping and Description | ICD-9-CM Code |
|---|---|
| K01. Trisomy 13 | 758.1 |
| K02. Down Syndrome | 758.0 |
| K03. Trisomy 18 | 758.2 |
| L. Other and Unspecified Congenital Anomalies | 759 |
What is the ICD 10 code for trisomy 18?
Trisomy 18, unspecified. Q91.3 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
What is trisomy 21 syndrome?
Also known as trisomy 21 syndrome A disorder caused by the presence of an extra chromosome 21 and characterized by mental retardation and distinguishing physical features Chromosome disorder associated either with an extra chromosome 21 or an effective trisomy for chromosome 21; clinical manifestations include hypotonia, short stature,...
What is the ICD-9 code for diagnosis?
ICD-9-CM 758.0 is a billable medical code that can be used to indicate a diagnosis on a reimbursement claim, however, 758.0 should only be used for claims with a date of service on or before September 30, 2015.
What is chromosomal abnormality?
Complete trisomy 18 syndrome. Trisomy 18, complete. Clinical Information. A chromosomal abnormality consisting of the presence of a third copy of chromosome 18 in somatic cells. A kind of genetic disease.
When will the ICD-10-CM Q91.3 be released?
The 2022 edition of ICD-10-CM Q91.3 became effective on October 1, 2021.
What is the ICD code for trisomy 18?
Q91.3 is a billable ICD code used to specify a diagnosis of trisomy 18, unspecified. A 'billable code' is detailed enough to be used to specify a medical diagnosis.
What is Edwards syndrome?
Edwards syndrome (also known as trisomy 18 [T18]) is a chromosomal abnormality caused by the presence of all, or part of, an extra 18th chromosome. This genetic condition almost always results from nondisjunction during meiosis. It is named after John Hilton Edwards, who first described the syndrome in 1960. It is the second-most common autosomal trisomy, after Down syndrome, that carries to term.
The ICD code Q910 is used to code Edwards syndrome
Edwards syndrome (also known as trisomy 18 [T18]) is a chromosomal abnormality caused by the presence of all, or part of, an extra 18th chromosome. This genetic condition almost always results from nondisjunction during meiosis. It is named after John Hilton Edwards, who first described the syndrome in 1960.
ICD-10-CM Alphabetical Index References for 'Q91.0 - Trisomy 18, nonmosaicism (meiotic nondisjunction)'
The ICD-10-CM Alphabetical Index links the below-listed medical terms to the ICD code Q91.0. Click on any term below to browse the alphabetical index.
Equivalent ICD-9 Code GENERAL EQUIVALENCE MAPPINGS (GEM)
This is the official approximate match mapping between ICD9 and ICD10, as provided by the General Equivalency mapping crosswalk. This means that while there is no exact mapping between this ICD10 code Q91.0 and a single ICD9 code, 758.2 is an approximate match for comparison and conversion purposes.
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