D72.0 — Genetic anomalies of leukocytes
Is D72.0 billable?
Yes — D72.0 is billable for FY2027. D72.0 is a valid, billable ICD-10-CM code at the highest level of specificity in its branch. D72.0 may be submitted for encounters from October 1, 2026 through September 30, 2027.
D72.0 at a glance
| Code | D72.0 |
|---|---|
| Description | Genetic anomalies of leukocytes |
| Billable | Yes |
| Code set | ICD-10-CM FY2027 |
| Valid for encounters | October 1, 2026 – September 30, 2027 |
Which MS-DRGs does D72.0 group to?
D72.0 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
How is D72.0 listed in the Alphabetic Index?
These are the routes through the Alphabetic Index that lead to D72.0. They show the wording a clinician may have documented, which often differs from the Tabular description.
- Alder (-Reilly) anomaly or syndrome (leukocyte granulation)
- Dohle body panmyelopathic syndrome
- Hegglin's anomaly or syndrome
- Hypersegmentation, leukocytic, hereditary
- Hyposegmentation, leukocytic, hereditary
- Jordan's anomaly or syndrome
- Leukomelanopathy, hereditary
- Mayanomaly or syndrome (-Hegglin)
- Neutrophilia, hereditary giant
- Pelger-Huët anomaly or syndrome
- Anomaly, anomalous › Alder (congenital) (unspecified type)
- Anomaly, anomalous › granulation or granulocyte, genetic (congenital) (unspecified type)
Excludes1 — never code together
The conditions below can never be reported together with D72.0 on the same claim. An Excludes1 note means the two conditions cannot occur in the same patient, so reporting both is a coding error.
- Chédiak (-Steinbrinck)-Higashi syndrome (E70.330)
Inclusion terms
Alternative wording in documentation that is classified to D72.0.
- Alder (granulation) (granulocyte) anomaly
- Alder syndrome
- Hereditary leukocytic hypersegmentation
- Hereditary leukocytic hyposegmentation
- Hereditary leukomelanopathy
- May-Hegglin (granulation) (granulocyte) anomaly
- May-Hegglin syndrome
- Pelger-Huët (granulation) (granulocyte) anomaly
- Pelger-Huët syndrome
Excludes1 — never code together — inherited from D72
The conditions below can never be reported together with D72.0 on the same claim. An Excludes1 note means the two conditions cannot occur in the same patient, so reporting both is a coding error.
Excludes2 — not included here — inherited from Chapter 3
The conditions below are not part of D72.0, but a patient may have both at the same time. When documentation supports it, D72.0 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 D72
The conditions below are not part of D72.0, but a patient may have both at the same time. When documentation supports it, D72.0 and the excluded code may both be reported.
- neutropenia (D70)
How long has D72.0 existed?
D72.0 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.