Congenital malformation syndromes predominantly involving limbs
Billable / specificPOA exempt
Q87.2 is a billable, specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes in FY2027.
Inclusion terms
Applicable to
- Holt-Oram syndrome
- Klippel-Trenaunay-Weber syndrome
- Nail patella syndrome
- Rubinstein-Taybi syndrome
- Sirenomelia syndrome
- Thrombocytopenia with absent radius [TAR] syndrome
- VATER syndrome
Includes (from Q87)
- Note: Codes from this chapter are not for use on maternal records
Excludes2
Not included here — may be reported together when both conditions exist.
Use additional code
Add a code to identify the following, if applicable.
- code(s) to identify all associated manifestations (from Q87)
Also known as
- Holt-Oram syndrome
- Klippel-Trenaunay-Weber syndrome
- Nail patella syndrome
- Rubinstein-Taybi syndrome
- Sirenomelia syndrome
- Thrombocytopenia with absent radius [TAR] syndrome
- VATER syndrome
- Fong's syndrome
- Klippel-Trenaunaysyndrome
- Mietens' syndrome
- Nail, patella syndrome
- Onycho-osteodysplasia
- Osteo-onycho-arthro-dysplasia
- Osteo-onychodysplasia, hereditary
- Österreicher-Turner syndrome
- Sirenomelia
- Syndrome, Fong's
- Syndrome, nail patella
- Syndrome, Osterreicher-Turner
- Syndrome, sirenomelia
Parent code
- Q87Other specified congenital malformation syndromes affecting multiple systemsHeader
Related codes
- Q87.0Congenital malformation syndromes predominantly affecting facial appearanceBillable
- Q87.1Congenital malformation syndromes predominantly associated with short statureHeader
- Q87.3Congenital malformation syndromes involving early overgrowthBillable
- Q87.4Marfan syndromeHeader
- Q87.5Other congenital malformation syndromes with other skeletal changesBillable
- Q87.8Other specified congenital malformation syndromes, not elsewhere classifiedHeader
- Q87.ALoeys-Dietz syndromeBillable