ICD-10-CM Code Q87.1
Congenital malformation syndromes predominantly associated with short stature
Billable CodeBillable codes are sufficient justification for admission to an acute care hospital when used a principal diagnosis.
POA Exempt CodeThe 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.
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:
|Indicator||Meaning||CMS Will Pay CC/MCC DRG Costs|
|Y||Diagnosis was present at time of inpatient admission||Yes|
|N||Diagnosis was not present at time of inpatient admission||No|
|U||Documentation insufficient to determine if the condition was present at the time of inpatient admission.||No|
|W||Clinically undetermined. Provider unable to clinically determine whether the condition was present at the time of inpatient admission.||Yes|
|1||Exempt from POA reporting||No|
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.
|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|
Coding Notes for Q87.1 Info for medical coders on how to properly use this ICD-10 code
Inclusion TermsInclusion 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
- 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)
- SjÃ¶gren-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.
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 Q87.1 and a single ICD9 code, 759.81 is an approximate match for comparison and conversion purposes.