results found in ( seconds)
We are looking for ways to improve. If you have an suggestion for how ICD.Codes could be better, submit your idea!

ICD-10-CM Code Q87.1
Congenital malformation syndromes predominantly associated with short stature

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

Q87.1 is a billable ICD code used to specify a diagnosis of congenital malformation syndromes predominantly associated with short stature. 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 Q871 is used to code Langer mesomelic dysplasia

langer mesomelic dysplasia (lmd) is a rare congenital disorder characterized by an altered bone formation that causes a severe short and disproportionate stature.

Specialty: Medical Genetics
MeSH Codes: , D016111, D016111, C535331, D011218, , D009456, , , D003057, C537533, C537534, C563881, D056730,
ICD 9 Codes: , 757.1, 757.120, 759.89, 759.81, , , , , 759.8, 759.89, 759.89, 759.89, 759.89, 759.89
Source: Wikipedia

Coding Notes for Q87.1 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.
Aarskog syndrome
Cockayne syndrome
De Lange syndrome
Dubowitz syndrome
Noonan syndrome
Prader-Willi syndrome
Robinow-Silverman-Smith syndrome
Russell-Silver syndrome
Seckel syndrome
Code Type-1 Excludes:
Type-1 Excludes
Type-1 Excludes mean the conditions excluded are mutually exclusive and should never be coded together. Excludes 1 means "do not code here."
Ellis-van Creveld syndrome - instead, use code Q77.6
Smith-Lemli-Opitz syndrome - instead, use code E78.72

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

  • Smith-Lemli-Opitz syndrome (disorder)
  • Pericarditis secondary to Mulibrey nanism (disorder)
  • Prader-Willi syndrome (disorder)
  • Sjögren-Larsson syndrome (disorder)

Coding Advice SNOMET-CT

  • Consider additional code to identify specific condition or disease

ICD-10-CM Alphabetical Index References for 'Q87.1 - Congenital malformation syndromes predominantly associated with short stature'

The ICD-10-CM Alphabetical Index links the below-listed medical terms to the ICD code Q87.1. Click on any term below to browse the alphabetical index.

Weil(l)-Marchesani syndrome (Q87.1)
Ullrich(-Bonnevie)(-Turner) syndrome (Q87.1)
Turner-like syndrome (Q87.1)
Seckel's syndrome (Q87.1)
Silver's syndrome (Q87.1)
Sjögren-Larsson syndrome (Q87.1)
Robinow-Silvermann-Smith syndrome (Q87.1)
Russell-Silver syndrome (Q87.1)
Prader-Willi syndrome (Q87.1)
Noonan's syndrome (Q87.1)
De Lange's syndrome (Q87.1)
Dubowitz' syndrome (Q87.1)
Cockayne's syndrome (Q87.1)
Cornelia de Lange syndrome (Q87.1)
Bonnevie-Ullrich syndrome (Q87.1)
Bruck-de Lange disease (Q87.1)
Aarskog's syndrome (Q87.1)
Amsterdam dwarfism (Q87.1)


Prader-Willi syndrome (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 Q87.1 and a single ICD9 code, 759.81 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/Q871