D82.1 — Di George's syndrome
Is D82.1 billable?
Yes — D82.1 is billable for FY2027. D82.1 is a valid, billable ICD-10-CM code at the highest level of specificity in its branch. D82.1 may be submitted for encounters from October 1, 2026 through September 30, 2027.
D82.1 at a glance
| Code | D82.1 |
|---|---|
| Description | Di George's syndrome |
| Billable | Yes |
| Code set | ICD-10-CM FY2027 |
| Valid for encounters | October 1, 2026 – September 30, 2027 |
Which MS-DRGs does D82.1 group to?
D82.1 sits in MDC 16 and helps define the logic of 3 MS-DRGs (version 44, FY2027). Which one a stay actually groups to also depends on procedures and secondary diagnoses.
- 808Major Hematological and Immunological Diagnoses Except Sickle Cell Crisis and Coagulation Disorders with MCCmedical
- 809Major Hematological and Immunological Diagnoses Except Sickle Cell Crisis and Coagulation Disorders with CCmedical
- 810Major Hematological and Immunological Diagnoses Except Sickle Cell Crisis and Coagulation Disorders without CC/MCCmedical
As a secondary diagnosis, D82.1 is a complication or comorbidity (CC), which can move a stay into a higher-paying DRG.
How is D82.1 listed in the Alphabetic Index?
These are the routes through the Alphabetic Index that lead to D82.1. They show the wording a clinician may have documented, which often differs from the Tabular description.
- Alymphoplasia, thymic
- Di George's syndrome
- DiGeorge's syndrome (thymic hypoplasia)
- Pharyngeal pouch syndrome
- Alymphocytosis › thymic
- Aplasia › parathyroid-thymic
- Aplasia › thymic, with immunodeficiency
- Dysplasia › thymic, with immunodeficiency
- Hypoplasia, hypoplastic › thymic, with immunodeficiency
- Syndrome › di George's
- Syndrome › pharyngeal pouch
- Hypoplasia, hypoplastic › thymus › with immunodeficiency
Inclusion terms
Alternative wording in documentation that is classified to D82.1.
- Pharyngeal pouch syndrome
- Thymic alymphoplasia
- Thymic aplasia or hypoplasia with immunodeficiency
Excludes1 — never code together — inherited from D80-D89
The conditions below can never be reported together with D82.1 on the same claim. An Excludes1 note means the two conditions cannot occur in the same patient, so reporting both is a coding error.
Excludes1 — never code together — inherited from D82
The conditions below can never be reported together with D82.1 on the same claim. An Excludes1 note means the two conditions cannot occur in the same patient, so reporting both is a coding error.
- ataxia telangiectasia [Louis-Bar] (G11.3)
Excludes2 — not included here — inherited from Chapter 3
The conditions below are not part of D82.1, but a patient may have both at the same time. When documentation supports it, D82.1 and the excluded code may both be reported.
- autoimmune disease (systemic) NOS (M35.9)
- certain conditions originating in the perinatal period (P00-P96)
- complications of pregnancy, childbirth and the puerperium (O00-O9A)
- congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
- endocrine, nutritional and metabolic diseases (E00-E88)
- human immunodeficiency virus [HIV] disease (B20)
- injury, poisoning and certain other consequences of external causes (S00-T88)
- neoplasms (C00-D49)
- symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94)
Excludes2 — not included here — inherited from D80-D89
The conditions below are not part of D82.1, but a patient may have both at the same time. When documentation supports it, D82.1 and the excluded code may both be reported.
- human immunodeficiency virus [HIV] disease (B20)
How long has D82.1 existed?
D82.1 has been in ICD-10-CM since at least FY2016, the earliest fiscal year on record here.
Derived from the official order files for FY2016–FY2026. FY2017 and FY2020 publish no order file, so those years are not covered.
Which codes are confused with D82.1?
ICD-10-CM declares these codes mutually exclusive with D82.1 — exactly one of each pair can be correct for a given encounter.
Which conditions are coded to D82.1?
What other codes are in the D82 family? (6)
- D82.0Wiskott-Aldrich syndrome
- D82.2Immunodeficiency with short-limbed stature
- D82.3Immunodeficiency following hereditary defective response to Epstein-Barr virus
- D82.4Hyperimmunoglobulin E [IgE] syndrome
- D82.8Immunodeficiency associated with other specified major defects
- D82.9Immunodeficiency associated with major defect, unspecified