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ICD-10-CM Code D72.0
Genetic anomalies of leukocytes

Billable Code
Billable codes are sufficient justification for admission to an acute care hospital when used a principal diagnosis.
| ICD-10 from 2011 - 2016

D72.0 is a billable ICD code used to specify a diagnosis of genetic anomalies of leukocytes. A 'billable code' is detailed enough to be used to specify a medical diagnosis.

The ICD code D720 is used to code May-Hegglin anomaly

May–Hegglin anomaly (MHA), also known as Dohle leukocyte inclusions with giant platelets and macrothrombocytopenia with leukocyte inclusions, is a rare genetic disorder of the blood platelets that causes them to be abnormally large.

Specialty: Hematology
ICD 9 Code: 288.2

Source: Wikipedia

Coding Notes for D72.0 Info for medical coders on how to properly use this ICD-10 code

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.
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
Code Type-1 Excludes:
Type-1 Excludes
Type-1 Excludes mean the conditions excluded are mutually exclusive and should never be coded together. Excludes 1 means "do not code here."
Chédiak (-Steinbrinck)-Higashi syndrome - instead, use code E70.330

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 'D72.0 - Genetic anomalies of leukocytes'

The ICD-10-CM Alphabetical Index links the below-listed medical terms to the ICD code D72.0. Click on any term below to browse the alphabetical index.

Pelger-Huët anomaly or syndrome (D72.0)
Neutrophilia, hereditary giant (D72.0)
May(-Hegglin) anomaly or syndrome (D72.0)
Leukomelanopathy, hereditary (D72.0)
Jordan's anomaly or syndrome (D72.0)
Hegglin's anomaly or syndrome (D72.0)
Hypersegmentation, leukocytic, hereditary (D72.0)
Hyposegmentation, leukocytic, hereditary (D72.0)
Dohle body panmyelopathic syndrome (D72.0)


Genetic anomalies of leukocytes (exact match)

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 288.2 was previously used, D72.0 is the appropriate modern ICD10 code.

Parent Code: D72 - Other disorders of white blood cells

** This Document Provided By ICD.Codes **
Source: http://icd.codes/icd10cm/D720