D72.0
BillableGenetic anomalies of leukocytes
Genetic anomalies of leukocytes
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
- 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)
Also Known As / Clinical Terms
SNOMED CT
- Combined immunodeficiency associated with maturation pathway defect3439009
- SCID (severe combined immunodeficiency) due to absent peripheral T cell maturation3439009
- Severe combined immunodeficiency due to absent peripheral T cell maturation3439009
- Pelger-Huet cell15111002
- Pelger-Huët cell15111002
- Genetic anomaly of leucocyte47986005
- Genetic anomaly of leukocyte47986005
- Genetic leucocyte disorder47986005
- Genetic leukocyte disorder47986005
- Pelger Huet anomaly85559002
- Pelger-Huet anomaly85559002
- Pelger-Huët anomaly85559002
- Congenital aleukia111584000
- De Vaal disease111584000
- Generalised haematopoietic hypoplasia111584000
- Generalized hematopoietic hypoplasia111584000
- Immunoerythromyeloid hypoplasia111584000
- Reticular dysgenesia111584000
- Reticular dysgenesis111584000
- SCID - Severe combined immunodeficiency, neutropaenia and thrombocytopaenia111584000
- SCID - Severe combined immunodeficiency, neutropenia and thrombocytopenia111584000
- Severe combined immunodeficiency, neutropaenia and thrombocytopaenia111584000
- Severe combined immunodeficiency, neutropenia and thrombocytopenia111584000
- Hereditary neutrophilia129639005
- Neutrophil count above reference range165518003
- Neutrophilia165518003
- Neutrophilic leucocytosis165518003
- Neutrophilic leukocytosis165518003
- Hereditary hypersegmentation234435002
- Defective phagocytic cell adhesion234581004
- LAD - Leucocyte adhesion deficiency type 1234582006
- LAD - Leukocyte adhesion deficiency type 1234582006
- LFA-1 deficiency234582006
- Leucocyte adhesion deficiency - type 1234582006
- Leucocyte adhesion molecule deficiency - type 1234582006
- Leukocyte adhesion deficiency - type 1234582006
- Leukocyte adhesion molecule deficiency - type 1234582006
- Mo-1 deficiency234582006
- Congenital disorder of glycosylation type IIc234583001
- LAD - Leucocyte adhesion deficiency type 2234583001
- LAD - Leukocyte adhesion deficiency type 2234583001
- Leucocyte adhesion deficiency - type 2234583001
- Leucocyte adhesion molecule deficiency - type 2234583001
- Leukocyte adhesion deficiency - type 2234583001
- Leukocyte adhesion molecule deficiency - type 2234583001
- Sialyl-Lewis X defect234583001
- Combined phagocytic defect234591005
- Hypersegmentation250275007
- De Vaal syndrome350353007
- De Vaal's syndrome350353007
- Immunodeficiency with generalised haematopoietic hypoplasia350353007
- Immunodeficiency with generalized hematopoietic hypoplasia350353007
- Reticular dysgenesis with congenital aleucocytosis351287008
- Reticular dysgenesis with congenital aleukocytosis351287008
- Neutrocytosis414850009
- Neutrophilia disorder414850009
- Congenital atrophy of optic nerve722990003
- Congenital optic atrophy722990003
- Leucocyte adherence deficiency1187233008
- Leucocyte adhesion deficiency1187233008
- Leukocyte adherence deficiency1187233008
- Leukocyte adhesion deficiency1187233008
- SOPH (short stature, optic nerve atrophy, Pelger-Huët anomaly) syndrome1237618009
- Short stature, optic nerve atrophy, Pelger-Huët anomaly syndrome1237618009
- LAD-1 (leucocyte adhesion deficiency-1) variant1269277004
- LAD-1 (leukocyte adhesion deficiency-1) variant1269277004
- LAD-III - leucocyte adhesion deficiency type III1269277004
- LAD-III - leukocyte adhesion deficiency type III1269277004
- Leucocyte adhesion deficiency type III1269277004
- Leucocyte adhesion deficiency-1 variant1269277004
- Leukocyte adhesion deficiency type 31269277004
- Leukocyte adhesion deficiency type III1269277004
- Leukocyte adhesion deficiency-1 variant1269277004
UMLS
- Alder (granulation) (granulocyte) anomalyC2873814
- Alder syndromeC1527030
- Begnez Cesar diseaseC0007965
- Beguez Cesar diseaseC0007965
- Béguez César diseaseC0007965
- CHEDIAK-HIGASHI SYNDROMEC0007965
- CHSC0007965
- Chediak Higashi SyndromeC0007965
- Chediak Higashi anomalyC0007965
- Chediak Higashi syndromeC0007965
- Chediak Steinbrinck Higashi SyndromeC0007965
- Chediak anomalyC0007965
- Chediak-Higashi SyndromeC0007965
- Chediak-Higashi syndromeC0007965
- Chediak-Steinbrinck anomalyC0007965
- Chediak-Steinbrinck-Higashi SyndromeC0007965
- Chediak-Steinbrinck-Higashi SyndromesC0007965
- Chediak-Steinbrinck-Higashi syndromeC0007965
- Chédiak anomalyC0007965
- Chédiak-Higashi syndromeC0007965
- Chédiak-Higashi syndrome (disorder)C0007965
- Chédiak-Steinbrinck anomalyC0007965
- Congenital gigantism of peroxidase granulesC0007965
- Granulation anomaly of leucocytesC0007965
- Granulation anomaly of leukocytesC0007965
- Hereditary gigantism of cytoplasmic organellesC0007965
- Hereditary leukomelanopathyC0007965
- Oculocutaneous Albinism with Leukocyte DefectC0007965
- Oculocutaneous albinism with leukocyte defectC0007965
- Steinbrinck anomalyC0007965
- chediak higashi anomalyC0007965
- chediak higashi syndromeC0007965
- chediak-higashi syndromeC0007965
- Congenital Leucocyte AbnormalityC0017377
- Congenital Leucocyte AnomalyC0017377
- Congenital Leukocyte AbnormalityC0017377
- Congenital Leukocyte AnomalyC0017377
- Genetic Anomaly of LeucocyteC0017377
- Genetic Anomaly of LeukocyteC0017377
- Genetic anomalies of leucocytesC0017377
- Genetic anomalies of leukocytesC0017377
- Genetic anomaly of leucocyteC0017377
- Genetic anomaly of leukocyteC0017377
- Genetic anomaly of leukocyte (disorder)C0017377
- Genetic leucocyte disorderC0017377
- Genetic leukocyte disorderC0017377
- Hereditary leukocytic hypersegmentationC1400046
- Hereditary leukocytic hyposegmentationC1400295
- May-Hegglin (granulation) (granulocyte) anomalyC2873815
- May-Hegglin AnomalyC0340978
- May-Hegglin anomalyC0340978
- May-Hegglin syndromeC0340978
- Pelger-Huët (granulation) (granulocyte) anomalyC2873816
- Pelger-Huët syndromeC0281938
Frequently Asked Questions
What is ICD-10 code D72.0?
ICD-10-CM code D72.0 represents "Genetic anomalies of leukocytes". It 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.
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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.