ICD-10-CM Code D82.1
Di George's syndrome
Billable Code
Billable codes are sufficient justification for admission to an acute care hospital when used a principal diagnosis.D82.1 is a billable ICD code used to specify a diagnosis of di George's syndrome. A 'billable code' is detailed enough to be used to specify a medical diagnosis.
The ICD code D821 is used to code DiGeorge syndrome
DiGeorge syndrome is also known as 22q11.2 deletion syndrome,DiGeorge anomaly, velocardiofacial syndrome (VCFS), Shprintzen syndrome, conotruncal anomaly face syndrome (CTAF) or Takao syndrome, Sedlackova syndrome, Cayler cardiofacial syndrome, Strong syndrome, congenital thymic aplasia, and thymic hypoplasia. This syndrome is caused by the deletion of a small piece of chromosome 22. As such, it is recommended that the name "22q11.2 deletion syndrome (22q11.2DS)" be used.
Specialty: | Medical Genetics |
MeSH Codes: | D004062, D004062 |
ICD 9 Codes: | 279.11, 758.32 |
Brain computer tomography cuts of the patient, demonstrating basal ganglia and periventricular calcification. From a case report by Tonelli et al., 2007
Coding Notes for D82.1 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. - Pharyngeal pouch syndrome
- Thymic alymphoplasia
- Thymic aplasia or hypoplasia with immunodeficiency
MS-DRG Mapping
- DRG Group #808-810 - Major hematol or immun diagnoses except sickle cell crisis and coagul with MCC.
- DRG Group #808-810 - Major hematol or immun diagnoses except sickle cell crisis and coagul with CC.
- DRG Group #808-810 - Major hematol or immun diagnoses except sickle cell crisis and coagul without CC or MCC.
ICD-10-CM Alphabetical Index References for 'D82.1 - Di George's syndrome'
The ICD-10-CM Alphabetical Index links the below-listed medical terms to the ICD code D82.1. Click on any term below to browse the alphabetical index.
Equivalent ICD-9 Code GENERAL EQUIVALENCE MAPPINGS (GEM)
This is the official exact match mapping between ICD9 and ICD10, as provided by the General Equivalency mapping crosswalk. This means that in all cases where the ICD9 code 279.11 was previously used, D82.1 is the appropriate modern ICD10 code.
Parent Code: D82 - Immunodeficiency associated with other major defects