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ICD-10-CM Code Q93.0
Whole chromosome monosomy, nonmosaicism (meiotic nondisjunction)

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

Q93.0 is a billable ICD code used to specify a diagnosis of whole chromosome monosomy, nonmosaicism (meiotic nondisjunction). 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 Q93 is used to code 22q13 deletion syndrome

22q13 deletion syndrome (spoken as twenty-two q one three) is a genetic disorder caused by deletions or rearrangements on the q terminal end (long arm) of chromosome 22. Any abnormal genetic variation in the q13 region that presents with significant manifestations (phenotype) typical of a terminal deletion should be diagnosed as 22q13 deletion syndrome. 22q13 deletion syndrome is often placed in the more general category of Phelan-McDermid Syndrome (abbreviated PMS), which includes some mutations and microdeletions. The PMS name is less precise, since there is disagreement among researchers as to which variants belong in the PMS category. The Developmental Synaptopathies Consortium defines PMS as being caused by SHANK3 mutations, a definition that excludes terminal deletions. This latter definition of PMS is incompatible with the defintion of 22q13 deletion syndrome by those who first described 22q13 deletion syndrome.

Specialty: Medical Genetics
MeSH Codes: C536801, D009006
ICD 9 Codes: ,
Source: Wikipedia

MS-DRG Mapping

  • DRG Group #951 - Other factors influencing health status.

ICD-10-CM Alphabetical Index References for 'Q93.0 - Whole chromosome monosomy, nonmosaicism (meiotic nondisjunction)'

The ICD-10-CM Alphabetical Index links the below-listed medical terms to the ICD code Q93.0. Click on any term below to browse the alphabetical index.

Equivalent ICD-9 Code GENERAL EQUIVALENCE MAPPINGS (GEM)

Other conditions due to autosomal 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 Q93.0 and a single ICD9 code, 758.5 is an approximate match for comparison and conversion purposes.


Parent Code: Q93 - Monosomies and deletions from the autosomes, not elsewhere classified

** This Document Provided By ICD.Codes **
Source: http://icd.codes/icd10cm/Q930