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Code
Description

ICD-10-CM Code Q87.2
Congenital malformation syndromes predominantly involving limbs

BILLABLE
Billable Code
Billable codes are sufficient justification for admission to an acute care hospital when used a principal diagnosis.
POA Exempt
POA Exempt Code
The Center for Medicare & Medicaid Services (CMS) requires medical coders to indicate whether or not a condition was present at the time of admission, in order to properly assign MS-DRG codes. This "Present On Admission" (POA) indicator is recorded on CMS form 4010A.
| ICD-10 from 2011 - 2016

Q87.2 is a billable ICD code used to specify a diagnosis of congenital malformation syndromes predominantly involving limbs. A 'billable code' is detailed enough to be used to specify a medical diagnosis.

POA Indicators on CMS form 4010A are as follows:

IndicatorMeaningCMS Will Pay CC/MCC DRG Costs
YDiagnosis was present at time of inpatient admissionYes
NDiagnosis was not present at time of inpatient admissionNo
UDocumentation insufficient to determine if the condition was present at the time of inpatient admission.No
WClinically undetermined. Provider unable to clinically determine whether the condition was present at the time of inpatient admission.Yes
1Exempt from POA reportingNo


The ICD code Q872 is used to code Holt-Oram syndrome

Holt–Oram syndrome is an autosomal dominant disorder that affects bones in the arms and hands (the upper limbs) and may also cause heart problems. The syndrome includes an absent radial bone in the arms, an atrial septal defect, and a first degree heart block. Holt–Oram syndrome is considered to be a phenocopy of thalidomide, since both the genetic disorder and the teratogenic effects have similar presentations in individuals.

Specialty: Medical Genetics
MeSH Codes: ,
ICD 9 Codes: , 287.33

Coding Notes for Q87.2 Info for medical coders on how to properly use this ICD-10 code

Inclusion Terms:
Inclusion Terms
Inclusion Terms are a list of concepts for which a specific code is used. The list of Inclusion Terms is useful for determining the correct code in some cases, but the list is not necessarily exhaustive.
Holt-Oram syndrome
Klippel-Trenaunay-Weber syndrome
Nail patella syndrome
Rubinstein-Taybi syndrome
Sirenomelia syndrome
Thrombocytopenia with absent radius [TAR] syndrome
VATER syndrome

MS-DRG Mapping

  • DRG Group #564-566 - Other musculoskeletal system and connective tissue diagnoses with MCC.
  • DRG Group #564-566 - Other musculoskeletal system and connective tissue diagnoses with CC.
  • DRG Group #564-566 - Other musculoskeletal system and connective tissue diagnoses without CC or MCC.

Related Concepts SNOMET-CT

  • Rubinstein-Taybi syndrome (disorder)
  • Klippel-Trenaunay-Weber syndrome (disorder)
  • Radial aplasia-thrombocytopenia syndrome (disorder)

Coding Advice SNOMET-CT

  • Consider additional code to identify specific condition or disease

ICD-10-CM Alphabetical Index References for 'Q87.2 - Congenital malformation syndromes predominantly involving limbs'

The ICD-10-CM Alphabetical Index links the below-listed medical terms to the ICD code Q87.2. Click on any term below to browse the alphabetical index.

VATER syndrome (Q87.2)
TAR(thrombocytopenia with absent radius) syndrome (Q87.2)
Taybi's syndrome (Q87.2)
Sirenomelia(syndrome) (Q87.2)
Rubinstein-Taybi syndrome (Q87.2)
Österreicher-Turner syndrome (Q87.2)
Mietens' syndrome (Q87.2)
Klippel-Trenaunay(-Weber) syndrome (Q87.2)
Holt-Oram syndrome (Q87.2)

Equivalent ICD-9 Code GENERAL EQUIVALENCE MAPPINGS (GEM)

Other specified congenital anomalies (approximate match)

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 Q87.2 and a single ICD9 code, 759.89 is an approximate match for comparison and conversion purposes.


Parent Code: Q87 - Other specified congenital malformation syndromes affecting multiple systems

** This Document Provided By ICD.Codes **
Source: http://icd.codes/icd10cm/Q872