ICD-10-CM Code Q93.5
Other deletions of part of a chromosome
Billable Code
Billable codes are sufficient justification for admission to an acute care hospital when used a principal diagnosis.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.Q93.5 is a billable ICD code used to specify a diagnosis of other deletions of part of a chromosome. 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 Q935 is used to code 9q34 deletion syndrome
9q34 deletion syndrome, also known as kleefstra syndrome, is a rare genetic disorder. terminal deletions of chromosome 9q34 have been associated with childhood hypotonia, a distinctive facial appearance and developmental disability. the facial features typically described include arched eyebrows, small head circumference, midface hypoplasia, prominent jaw and a pouting lower lip. individuals with this disease may often have speech impediments, such as speech delays. other characteristics of this disease include: epilepsy, congenital and urogenetic defects, microcephaly, corpulence, and psychiatric disorders. from analysis of chromosomal breakpoints, as well as gene sequencing in suggestive cases, kleefstra and colleagues identified ehmt1 as the causative gene. this gene is responsible for producing the protein histone methyltransferase which functions to alter histones. ultimately, histone methyltransferases are important in deactivating certain genes, needed for proper growth and development. moreover, a frameshift, missense, or nonsense error in the coding sequence of ehmt1 can result in this condition in an individual.
| Specialty: | Medical Genetics |
| MeSH Codes: | , |
| ICD 9 Codes: | , 758.33 |
Coding Notes for Q93.5 Info for medical coders on how to properly use this ICD-10 code
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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. - Angelman syndrome
MS-DRG Mapping
- DRG Group #884 - Organic disturbances and mental retardation.
Related Concepts SNOMET-CT
- Sensorineural deafness and male infertility (disorder)
- 10p partial monosomy syndrome (disorder)
- 9p partial monosomy syndrome (disorder)
- 7q partial monosomy syndrome (disorder)
- 12p partial monosomy syndrome (disorder)
- 8q partial monosomy syndrome (disorder)
- 22q partial monosomy syndrome (disorder)
ICD-10-CM Alphabetical Index References for 'Q93.5 - Other deletions of part of a chromosome'
The ICD-10-CM Alphabetical Index links the below-listed medical terms to the ICD code Q93.5. 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 Q93.5 and a single ICD9 code, 758.39 is an approximate match for comparison and conversion purposes.
Parent Code: Q93 - Monosomies and deletions from the autosomes, not elsewhere classified