ICD-10-CM Code Q93.89
Other deletions from the autosomes
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.
Q93.89 is a billable ICD code used to specify a diagnosis of other deletions from the autosomes. 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 Q938 is used to code Williams syndrome
Williams syndrome (WS), also known as Williams–Beuren syndrome (WBS), is a rare neurodevelopmental disorder characterized by: a distinctive, "elfin" facial appearance, along with a low nasal bridge; an unusually cheerful demeanor and ease with strangers; developmental delay coupled with strong language skills; profound visuo-spatial impairments; and cardiovascular problems, such as supravalvular aortic stenosis and transient high blood calcium.
|Specialty:||Medical Genetics, Pediatrics|
|ICD 9 Code:||758.9|
Ten-year-old boy with Williams syndrome
Coding Notes for Q93.89 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.
- Deletions identified by fluorescence in situ hybridization (FISH)
- Deletions identified by in situ hybridization (ISH)
- Deletions seen only at prometaphase
- DRG Group #884 - Organic disturbances and mental retardation.
Related Concepts SNOMET-CT
- Monosomy 22 and absence of immunoglobulin A (disorder)
ICD-10-CM Alphabetical Index References for 'Q93.89 - Other deletions from the autosomes'
The ICD-10-CM Alphabetical Index links the below-listed medical terms to the ICD code Q93.89. 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 Q93.89 and a single ICD9 code, 758.39 is an approximate match for comparison and conversion purposes.
Parent Code: Q93.8 - Other deletions from the autosomes