AutoICD API

D72.0

Billable

Genetic anomalies of leukocytes

Genetic anomalies of leukocytes

Status

Billable / Specific

Block

D70-D77

Parent Code

D72

ICD-11 Mapping

1 equivalent

Coding Notes

Inclusion Terms

Alternative clinical terms for this condition

  • 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

Excludes 1

Codes that cannot be used together with this code (mutual exclusion)

Excludes 2

Conditions not included here, but the patient may have both

Related Codes(3)
D72.1

Eosinophilia

D72.8

Other specified disorders of white blood cells

D72.9

Disorder of white blood cells, unspecified

Billable
ICD-11 Equivalents(1)

ICD-11 Equivalents

View full mapping

Corresponding ICD-11 codes from the WHO crosswalk mapping

4B0ZImmune system disorders involving white cell lineages, unspecifiedequivalentPrimary
Also Known As / Clinical Terms(238)

SNOMED CT

UMLS

Clinical Terms

  • Pelger-Huet cell
  • Hereditary hypersegmentation
  • Severe combined immunodeficiency, neutropaenia and thrombocytopaenia
  • Congenital Leucocyte Anomaly
  • Genetic leukocyte disorder
  • Oculocutaneous Albinism with Leukocyte Defect
  • Chediak Higashi syndrome
  • Leukocyte adhesion molecule deficiency - type 2
  • Hereditary gigantism of cytoplasmic organelles
  • Severe combined immunodeficiency, neutropenia and thrombocytopenia
  • LAD-III - leucocyte adhesion deficiency type III
  • LAD - Leucocyte adhesion deficiency type 1
  • Chédiak-Higashi syndrome (disorder)
  • Congenital atrophy of optic nerve
  • LAD-III - leukocyte adhesion deficiency type III
  • May-Hegglin anomaly
  • De Vaal syndrome
  • May-Hegglin syndrome
  • Leucocyte adhesion molecule deficiency - type 1
  • SOPH (short stature, optic nerve atrophy, Pelger-Huët anomaly) syndrome
  • Hypersegmentation
  • Pelger-Huet anomaly
  • Leukocyte adhesion deficiency type III
  • Chédiak anomaly
  • Short stature, optic nerve atrophy, Pelger-Huët anomaly syndrome
  • Congenital Leukocyte Abnormality
  • Genetic anomaly of leukocyte
  • Genetic anomaly of leucocyte
  • SCID - Severe combined immunodeficiency, neutropaenia and thrombocytopaenia
  • Begnez Cesar disease
  • Genetic leucocyte disorder
  • Combined phagocytic defect
  • Reticular dysgenesis with congenital aleucocytosis
  • Pelger-Huët cell
  • chediak-higashi syndrome
  • LAD - Leucocyte adhesion deficiency type 2
  • Leucocyte adhesion deficiency - type 1
  • Leucocyte adhesion deficiency-1 variant
  • Pelger-Huët anomaly
  • Steinbrinck anomaly
  • Granulation anomaly of leucocytes
  • De Vaal's syndrome
  • Leukocyte adhesion deficiency type 3
  • LAD - Leukocyte adhesion deficiency type 2
  • Genetic anomalies of leucocytes
  • chediak higashi anomaly
  • Leukocyte adhesion deficiency - type 2
  • Sialyl-Lewis X defect
  • Generalised haematopoietic hypoplasia
  • Immunodeficiency with generalized hematopoietic hypoplasia
  • Leucocyte adhesion deficiency type III
  • Leukocyte adhesion deficiency - type 1
  • Neutrophilia disorder
  • Neutrophilic leucocytosis
  • Reticular dysgenesia
  • Reticular dysgenesis
  • Leukocyte adhesion deficiency-1 variant
  • Pelger-Huët (granulation) (granulocyte) anomaly
  • Chédiak-Steinbrinck anomaly
  • Chediak-Steinbrinck-Higashi Syndrome
  • SCID - Severe combined immunodeficiency, neutropenia and thrombocytopenia
  • De Vaal disease
  • Neutrophilic leukocytosis
  • Reticular dysgenesis with congenital aleukocytosis
  • Severe combined immunodeficiency due to absent peripheral T cell maturation
  • Genetic anomaly of leukocyte (disorder)
  • Granulation anomaly of leukocytes
  • Alder syndrome
  • Immunoerythromyeloid hypoplasia
  • Pelger-Huët syndrome
  • LAD - Leukocyte adhesion deficiency type 1
  • Chediak-Steinbrinck anomaly
  • Congenital optic atrophy
  • Hereditary neutrophilia
  • Beguez Cesar disease
  • Hereditary leukomelanopathy
  • Congenital Leucocyte Abnormality
  • Leucocyte adhesion deficiency - type 2
  • May-Hegglin (granulation) (granulocyte) anomaly
  • Mo-1 deficiency
  • Leucocyte adherence deficiency
  • Congenital Leukocyte Anomaly
  • Leukocyte adherence deficiency
  • Chediak-Steinbrinck-Higashi Syndromes
  • LAD-1 (leucocyte adhesion deficiency-1) variant
  • Leukocyte adhesion deficiency
  • Congenital gigantism of peroxidase granules
  • Combined immunodeficiency associated with maturation pathway defect
  • Immunodeficiency with generalised haematopoietic hypoplasia
  • CHS
  • Leucocyte adhesion deficiency
  • Chediak Steinbrinck Higashi Syndrome
  • Béguez César disease
  • Congenital disorder of glycosylation type IIc
  • Leukocyte adhesion molecule deficiency - type 1
  • LAD-1 (leukocyte adhesion deficiency-1) variant
  • Neutrophilia
  • Generalized hematopoietic hypoplasia
  • Chediak anomaly
  • Hereditary leukocytic hypersegmentation
  • Neutrocytosis
  • Chédiak-Higashi syndrome
  • Alder (granulation) (granulocyte) anomaly
  • SCID (severe combined immunodeficiency) due to absent peripheral T cell maturation
  • Defective phagocytic cell adhesion
  • Congenital aleukia
  • LFA-1 deficiency
  • Leucocyte adhesion molecule deficiency - type 2
  • Hereditary leukocytic hyposegmentation
  • Pelger Huet anomaly
  • Neutrophil count above reference range
Frequently Asked Questions
What is the ICD-10 code for genetic anomalies of leukocytes?

The ICD-10-CM code for genetic anomalies of leukocytes is D72.0. The full clinical description is "Genetic anomalies of leukocytes". D72.0 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code D72.0 mean?

ICD-10-CM code D72.0 represents “Genetic anomalies of leukocytes”. It is classified under Chapter 3: Diseases of the Blood and Blood-Forming Organs and is a billable/specific code that can be used on a claim.

Is D72.0 a billable code?

Yes, D72.0 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is D72.0 in?

D72.0 is in Chapter 3: Diseases of the Blood and Blood-Forming Organs (codes D50-D89).

What codes cannot be used with D72.0?

D72.0 has Excludes1 notes indicating codes that cannot be used together with it, including: basophilia (D72.824); immunity disorders (D80-D89); neutropenia (D70); and 2 more.

What SNOMED CT codes does D72.0 map to?

D72.0 maps to 20 SNOMED CT concepts: 3439009, 234591005, 111584000, 722990003, 234583001, and 15 more. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for D72.0?

D72.0 is linked to 10 UMLS Concept Unique Identifiers: C2873814, C1527030, C0007965, C0017377, C1400046, and 5 more. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does D72.0 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like genetic anomalies of leukocytes affect a person's functioning: body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.

What is the ICD-11 equivalent of D72.0?

D72.0 maps to the ICD-11 code: 4B0Z (Immune system disorders involving white cell lineages, unspecified).

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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.