R71.8
BillableOther abnormality of red blood cells
Other abnormality of red blood cells
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Abnormal red-cell morphology NOS
- Abnormal red-cell volume NOS
- Anisocytosis
- Poikilocytosis
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
- abnormal findings on antenatal screening of mother (O28.-)
- certain conditions originating in the perinatal period (P04-P96)
- signs and symptoms classified in the body system chapters
- signs and symptoms of breast (N63, N64.5)
- abnormalities of lipids (E78.-)
- abnormalities of platelets and thrombocytes (D69.-)
- abnormalities of white blood cells classified elsewhere (D70-D72)
- coagulation hemorrhagic disorders (D65-D68)
- diagnostic abnormal findings classified elsewhere - see Alphabetical Index
- hemorrhagic and hematological disorders of newborn (P50-P61)
Also Known As / Clinical Terms
SNOMED CT
- Decreased blood erythrocyte volume2634004
- Increased blood erythrocyte volume3570003
- Hereditary elliptocytosis due to deficiency of protein 4.15994005
- Hereditary elliptocytosis due to alpha spectrin defect8857001
- Severe hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin10564005
- Hereditary elliptocytosis due to glycophorin C deficiency15121005
- Intravascular haemolysis15601008
- Intravascular hemolysis15601008
- Decreased erythrocyte production18469004
- Dyserythropoiesis18661009
- Increased erythrocyte destruction20039003
- Mild hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin24975009
- Increased erythrocyte production25151000
- Hereditary spherocytosis due to spectrin deficiency25266006
- Mild hereditary spherocytosis due to spectrin deficiency32648007
- Hereditary spherocytosis due to deficiency of protein 4.233905008
- Decreased osmotic fragility37253000
- Extramedullary haematopoiesis42952007
- Extramedullary hematopoiesis42952007
- Hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin47516005
- Erythrocyte aggregation50311009
- Extravascular haemolysis51467008
- Extravascular hemolysis51467008
- Sensitised cell52976009
- Sensitized cell52976009
- Congenital spherocytic haemolytic anaemia55995005
- Congenital spherocytic hemolytic anemia55995005
- Congenital spherocytosis55995005
- Familial acholuric jaundice55995005
- Familial spherocytosis55995005
- HS - Hereditary spherocytosis55995005
- Hereditary spherocytosis55995005
- Minkowsky-Chauffard syndrome55995005
- Erythrocytic maturation arrest56894004
- Erythroid maturation arrest56894004
- RBC - red blood cell maturation arrest56894004
- RBC maturation arrest56894004
- Sensitised red cell57722009
- Sensitized red cell57722009
- Erythrophagia61070002
- Erythrophagocytosis61070002
- Haemocytophagia61070002
- Haemophagocytosis61070002
- Hemocytophagia61070002
- Hemophagocytosis61070002
- Decreased erythrocyte destruction61469009
- Hereditary elliptocytosis due to beta spectrin-ankyrin interaction66262001
- Hereditary spherocytosis due to beta spectrin defect69981004
- Ineffective erythropoiesis70730006
- Hereditary elliptocytosis due to beta spectrin defect in self-association73073009
- Megaloblastoid erythropoiesis73255003
- Haemolysis73320003
- Hemolysis73320003
- Increased osmotic fragility75083006
- Hereditary elliptocytosis due to abnormal protein 4.175443009
- Severe hereditary spherocytosis due to spectrin deficiency77413008
- Decreased erythrocyte life span78867009
- Abnormal erythrocyte maturation81869008
- Abnormal erythrocyte production81869008
- Abnormal erythrocyte destruction88492006
- Decreased haem-haem interaction88861003
- Decreased heme-heme interaction88861003
- Increased haem-haem interaction89327000
- Increased heme-heme interaction89327000
- Erythrocyte sequestration102278006
- Red blood cell sequestration102278006
- Extramedullary erythropoiesis124958002
- Siderocytophagocytosis124962008
- Erythrocyte life span finding127402007
- Folic acid above reference range131132008
- Increased folic acid131132008
- Decreased folic acid131133003
- Folic acid below reference range131133003
- Haemoglobin above reference range131141003
- Hemoglobin above reference range131141003
- Increased haemoglobin131141003
- Increased hemoglobin131141003
- Increased methaemoglobin131171006
- Increased methemoglobin131171006
- Methaemoglobin above reference range131171006
- Methemoglobin above reference range131171006
- Decreased methaemoglobin131172004
- Decreased methemoglobin131172004
- Methaemoglobin below reference range131172004
- Methemoglobin below reference range131172004
- Increased sulfhemoglobin131173009
- Increased sulphaemoglobin131173009
- Sulfhemoglobin above reference range131173009
- Sulphaemoglobin above reference range131173009
- Decreased sulfhemoglobin131174003
- Decreased sulphaemoglobin131174003
- Sulfhemoglobin below reference range131174003
- Sulphaemoglobin below reference range131174003
- Carboxyhaemoglobin above reference range131175002
- Carboxyhemoglobin above reference range131175002
- Increased carboxyhaemoglobin131175002
- Increased carboxyhemoglobin131175002
- Carboxyhaemoglobin below reference range131176001
- Carboxyhemoglobin below reference range131176001
- Decreased carboxyhaemoglobin131176001
- Decreased carboxyhemoglobin131176001
- Haematocrit above reference range165413005
- Haematocrit high165413005
- Hematocrit above reference range165413005
- Hematocrit high165413005
- PCV (packed cell volume) above reference range165413005
- PCV (packed cell volume) high165413005
- Haematocrit outside reference range165416002
- Hematocrit outside reference range165416002
- PCV (packed cell volume) abnormal165416002
- PCV (packed cell volume) outside reference range165416002
- Erythrocytopenia165423001
- Erythropenia165423001
- RBC count low165423001
- Red blood cell count below reference range165423001
- Red blood cell count low165423001
- RBC count raised165424007
- Red blood cell count above reference range165424007
- Red blood cell count raised165424007
- RBC (red blood cell) count abnormal165427000
- Red blood cell count abnormal165427000
- Red blood cell count outside reference range165427000
- Color index above reference range165432004
- Color index raised165432004
- Colour index above reference range165432004
- Colour index raised165432004
- Erythrocyte color index above reference range165432004
- Erythrocyte colour index above reference range165432004
- Color index below reference range165433009
- Color index low165433009
- Colour index below reference range165433009
- Colour index low165433009
- Erythrocyte color index below reference range165433009
- Erythrocyte colour index below reference range165433009
- MCH - low165439008
- Mean corpuscular haemoglobin (MCH) - low165439008
- Mean corpuscular haemoglobin below reference range165439008
- Mean corpuscular haemoglobin low165439008
- Mean corpuscular hemoglobin (MCH) - low165439008
- Mean corpuscular hemoglobin below reference range165439008
- Mean corpuscular hemoglobin low165439008
- MCH - raised165440005
- Mean corpuscular haemoglobin (MCH) - raised165440005
- Mean corpuscular haemoglobin above reference range165440005
- Mean corpuscular haemoglobin raised165440005
- Mean corpuscular hemoglobin (MCH) - raised165440005
- Mean corpuscular hemoglobin above reference range165440005
- Mean corpuscular hemoglobin raised165440005
- MCH - abnormal165442002
- Mean corpuscular haemoglobin (MCH) - abnormal165442002
- Mean corpuscular haemoglobin abnormal165442002
- Mean corpuscular haemoglobin outside reference range165442002
- Mean corpuscular hemoglobin (MCH) - abnormal165442002
- Mean corpuscular hemoglobin abnormal165442002
- Mean corpuscular hemoglobin outside reference range165442002
- MCHC - low165447008
- Mean corpuscular haemoglobin concentration (MCHC) - low165447008
- Mean corpuscular haemoglobin concentration below reference range165447008
- Mean corpuscular hemoglobin concentration (MCHC) - low165447008
- Mean corpuscular hemoglobin concentration - low165447008
- Mean corpuscular hemoglobin concentration below reference range165447008
- MCHC - raised165448003
- Mean corpuscular haemoglobin concentration (MCHC) - raised165448003
- Mean corpuscular haemoglobin concentration above reference range165448003
- Mean corpuscular haemoglobin concentration raised165448003
- Mean corpuscular hemoglobin concentration (MCHC) - raised165448003
- Mean corpuscular hemoglobin concentration above reference range165448003
- Mean corpuscular hemoglobin concentration raised165448003
- MCV - raised165454002
- Mean corpuscular volume - raised165454002
- Mean corpuscular volume above reference range165454002
- MCV - low165455001
- Mean corpuscular volume - low165455001
- Mean corpuscular volume below reference range165455001
- ESR (erythrocyte sedimentation rate) abnormal165465007
- Erythrocyte sedimentation rate abnormal165465007
- Erythrocyte sedimentation rate outside reference range165465007
- ESR low165466008
- Erythrocyte sedimentation rate (ESR) low165466008
- Erythrocyte sedimentation rate below reference range165466008
- Low erythrocyte sedimentation rate165466008
- Microcytosis165474009
- Microcytosis, red cells165474009
- Anisocytosis, red cells165475005
- RBC's - anisocytosis165475005
- Poikilocytosis165479004
- Hypochromic red blood cells165486007
- RBC's - megaloblasts165488008
- Red blood cells - megaloblasts165488008
- Polychromatic red blood cells165489000
- Auto-agglutination of red blood cell165495004
- Autoagglutination of red blood cell165495004
- Rouleaux165496003
- RBC enzymes abnormal165500001
- Red blood cell enzymes abnormal165500001
- TIBC - Total iron binding capacity low165630002
- Total iron binding capacity below reference range165630002
- Total iron binding capacity low165630002
- RBC folate low165656009
- Red blood cell folate below reference range165656009
- Red blood cell folate low165656009
- Red cell folate abnormal165661006
- Red cell folate outside reference range165661006
- Reticulocyte count abnormal165685003
- Reticulocyte count outside reference range165685003
- Congenital elliptocytosis191169008
- HE - hereditary elliptocytosis191169008
- Hereditary elliptocytosis191169008
- Hereditary ovalocytosis191169008
- Erythrocyte membrane abnormality234409003
- Hereditary elliptocytosis with transient poikilocytosis234410008
- Sickling test positive250225005
- Red blood cell inclusions250233006
- Howell Jolly bodies250234000
- Pappenheimer bodies250235004
- Heinz bodies250236003
- Finding related to haemoglobin H inclusions250237007
- Finding related to hemoglobin H inclusions250237007
- Haemoglobin H inclusions250237007
- Hemoglobin H inclusions250237007
- Red blood cell population250239005
- Red blood cell population finding250239005
- Anisochromia250240007
- Dimorphic red blood cell population250240007
- Dacrocytosis250243009
- Teardrop cells250243009
- Pyknocytosis250244003
- Sputnik cells250246001
- Microspherocytes seen250252000
- Puddle cells250253005
- Ascorbate-cyanide detected by screening250264008
- Ascorbate-cyanide screening test positive250264008
- Sucrose haemolysis test positive250266005
- Sucrose hemolysis test positive250266005
- Sugar-water test positive250266005
- Ringed sideroblast259679003
- Alteration of haemoglobin concentration264777008
- Alteration of hemoglobin concentration264777008
- Finding of red blood cell staining275807006
- RBC staining275807006
- Red blood cell agglutination302783002
- Red blood cell clumping302783002
- Burr cells present313235003
- Finding of mean cell haemoglobin level365611000
- Finding of mean cell hemoglobin level365611000
- Mean cell haemoglobin level365611000
- Mean cell haemoglobin level - finding365611000
- Mean cell hemoglobin level365611000
- Mean cell hemoglobin level - finding365611000
- Finding of mean cell haemoglobin concentration365612007
- Finding of mean cell hemoglobin concentration365612007
- Mean cell haemoglobin concentration365612007
- Mean cell haemoglobin concentration - finding365612007
- Mean cell hemoglobin concentration365612007
- Mean cell hemoglobin concentration - finding365612007
- Finding of haematocrit - packed cell volume level365618006
- Finding of hematocrit - packed cell volume level365618006
- Haematocrit - PCV level365618006
- Haematocrit - PCV level - finding365618006
- Hematocrit - PCV level365618006
- Hematocrit - PCV level - finding365618006
- Finding of red blood cell maturation age365620009
- Red blood cell maturation age365620009
- Red blood cell maturation age - finding365620009
- Finding of red blood cell size365622001
- Red blood cell size365622001
- Red blood cell size - finding365622001
- Finding of red blood cell color365623006
- Finding of red blood cell colour365623006
- Red blood cell color - finding365623006
- Red blood cell colour - finding365623006
- Color index level365624000
- Color index level - finding365624000
- Colour index level365624000
- Colour index level - finding365624000
- Erythrocyte color index365624000
- Erythrocyte colour index365624000
- Finding of color index level365624000
- Finding of colour index level365624000
- Erythrocyte sedimentation rate365649001
- Erythrocyte sedimentation rate - finding365649001
- Finding of erythrocyte sedimentation rate365649001
- Schistocytosis385472000
- Blister cells397050008
- Eccentrocytosis397054004
- Cabot ring bodies397062007
- Cabot's ring bodies397062007
- Basophilic stippling397063002
- Basophilic stippling, erythrocytes397063002
- Haemoglobin SC crystals397066005
- Hemoglobin SC crystals397066005
- Haemoglobin C crystals397067001
- Hemoglobin C crystals397067001
- Plasmodium merozoite in red cell397068006
- Plasmodium microgametocyte in red cell397069003
- Plasmodium macrogametocyte in red cell397070002
- Malarial red blood cell inclusion397071003
- Babesia red blood cell inclusion397072005
- Leptocytes398977003
- Leptocytosis398977003
- Target cells present398977003
- Abnormal red blood cell volume441791009
- Red blood cell volume outside reference range441791009
- Haemoglobin level outside reference range441793007
- Hemoglobin level outside reference range441793007
- Red blood cell morphology abnormal441973005
- Plasmodium malariae gametocyte in red cell699619009
- Increased erythrocyte ghost cells in blood703428006
- Delayed haemolysis following artesunate therapy870431002
- Delayed hemolysis following artesunate therapy870431002
- PADH - post-artesunate delayed haemolysis870431002
- PADH - post-artesunate delayed hemolysis870431002
- Post-artesunate delayed haemolysis870431002
- Post-artesunate delayed hemolysis870431002
- Red blood cell folate above reference range1179811002
- Presence of haemoglobin alpha-chain variant681401000119103
- Presence of hemoglobin alpha-chain variant681401000119103
- Presence of haemoglobin delta chain variant681421000119107
- Presence of hemoglobin delta chain variant681421000119107
- Presence of unidentified haemoglobin variant15758261000119106
- Presence of unidentified hemoglobin variant15758261000119106
UMLS
- Abnormal MCVC0853655
- Abnormal erythrocyte volumeC0853655
- Abnormal mean corpuscular volumeC0853655
- Abnormal red-cell volume NOSC0853655
- MCV abnormalC0853655
- Mean cell volume abnormalC0853655
- Mean cell volume abnormal NOSC0853655
- Mean corpuscular volume abnormalC0853655
- abnormal mcvC0853655
- mcv abnormalC0853655
- Abnormal red cell morphologyC0476320
- Abnormal red-cell morphology NOSC0476320
- Red blood cell morphology NOS abnormalC0476320
- Red blood cell morphology abnormalC0476320
- Red blood cell morphology abnormal (finding)C0476320
- AnisocytosisC0221278
- Anisocytosis (morphologic abnormality)C0221278
- Anisocytosis, red cellsC0221278
- Anisocytosis, red cells (finding)C0221278
- RBC's - anisocytosisC0221278
- Unequal size of red blood cellsC0221278
- anisocytosisC0221278
- Other abnormality of red blood cellsC0878708
- PoikilocytosisC0221281
- Poikilocytosis (finding)C0221281
- poikilocytosisC0221281
Frequently Asked Questions
What is ICD-10 code R71.8?
ICD-10-CM code R71.8 represents "Other abnormality of red blood cells". It is a billable/specific code that can be used on a claim.
Is R71.8 a billable code?
Yes, R71.8 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is R71.8 in?
R71.8 is in Chapter 18: Symptoms, Signs and Abnormal Clinical and Laboratory Findings (codes R00-R99).
What codes cannot be used with R71.8?
R71.8 has Excludes1 notes indicating codes that cannot be used together with it, including: anemias (D50-D64); anemia of premature infant (P61.2); benign (familial) polycythemia (D75.0); and 6 more.
What SNOMED CT codes does R71.8 map to?
R71.8 maps to 136 SNOMED CT concepts: 61070002, 88492006, 81869008, 441791009, 264777008, and 131 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for R71.8?
R71.8 is linked to 5 UMLS Concept Unique Identifiers: C0853655, C0476320, C0221278, C0878708, C0221281. 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.