D61.818
BillableOther pancytopenia
Other pancytopenia
Coding Notes
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
- pancytopenia (due to) (with) aplastic anemia (D61.9)
- pancytopenia (due to) (with) bone marrow infiltration (D61.82)
- pancytopenia (due to) (with) congenital (pure) red cell aplasia (D61.01)
- pancytopenia (due to) (with) hairy cell leukemia (C91.4-)
- pancytopenia (due to) (with) human immunodeficiency virus disease (B20.-)
- pancytopenia (due to) (with) leukoerythroblastic anemia (D61.82)
- pancytopenia (due to) (with) myeloproliferative disease (D47.1)
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)
- neutropenia (D70.-)
- pancytopenia (due to) (with) myelodysplastic syndromes (D46.-)
Also Known As / Clinical Terms
SNOMED CT
- Autoimmune pancytopenia183005
- Acquired pancytopenia5876000
- Pancytopenia - acquired5876000
- Doan-Wright syndrome38970002
- Splenic pancytopenia syndrome38970002
- Neonatal purpura82835005
- Neonatal thrombocytopenia82835005
- Purpura of newborn82835005
- Autoimmune leucopenia123777002
- Autoimmune leukopenia123777002
- Pancytopenia127034005
- Neonatal anaemia234350007
- Neonatal anemia234350007
- Pancytopenia with pancreatitis234367000
- Haemophagocytic lymphohistiocytosis234437005
- Haemophagocytic syndrome234437005
- Hemophagocytic lymphohistiocytosis234437005
- Hemophagocytic syndrome234437005
- Hyperinflammatory lymphohistiocytosis234437005
- Disorder of haematopoietic system in newborn414028007
- Disorder of hematopoietic system in newborn414028007
- Ataxia pancytopenia syndrome768556005
- Myelocerebellar disorder768556005
- Combined immunodeficiency due to IKAROS deficiency783142006
- Pancytopenia due to IKAROS family zinc finger 1 mutations783142006
- Pancytopenia due to IKZF1 mutations783142006
- NOCARH syndrome1360083000
- Neonatal onset cytopenia, autoinflammation, rash, episodes of hemophagocytic lymphohistiocytosis syndrome1360083000
Frequently Asked Questions
What is ICD-10 code D61.818?
ICD-10-CM code D61.818 represents "Other pancytopenia". It is a billable/specific code that can be used on a claim.
Is D61.818 a billable code?
Yes, D61.818 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is D61.818 in?
D61.818 is in Chapter 3: Diseases of the Blood and Blood-Forming Organs (codes D50-D89).
What codes cannot be used with D61.818?
D61.818 has Excludes1 notes indicating codes that cannot be used together with it, including: pancytopenia (due to) (with) aplastic anemia (D61.9); pancytopenia (due to) (with) bone marrow infiltration (D61.82); pancytopenia (due to) (with) congenital (pure) red cell aplasia (D61.01); and 4 more.
What SNOMED CT codes does D61.818 map to?
D61.818 maps to 13 SNOMED CT concepts: 5876000, 768556005, 123777002, 183005, 783142006, and 8 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for D61.818?
D61.818 is linked to 1 UMLS Concept Unique Identifier: C3161075. 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.