DB35 Polyp of large intestine International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2026-01 Polyps are abnormal growths rising from the lining of the large intestine that protrude into the intestinal lumen. Polyps can cause bleeding, and over time, can develop into cancers.
exclusions code elsewhere sections/codes in this section () postcoordination Add Stem and/or Extension codes to form a cluster code which adds detail to the condition.
Specific anatomy - multiple selections are allowed [select] XA6J68 Caecum XA3VB0 Ileocecal valve XA4F42 Ileocecal junction XA3AL5 Ascending colon XA95L3 Hepatic flexure of colon XA49U1 Transverse colon XA1PY9 Splenic flexure of colon XA2G13 Descending colon XA8YJ9 Sigmoid colon XA33J5 Rectosigmoid junction XA4KU2 Rectum XA41Y4 Upper rectum XA2P23 Middle rectum XA1LM5 Lower rectum Has manifestation - multiple selections are allowed [select] 3A50 Thalassaemias 3A51 Sickle cell disorders or other haemoglobinopathies 3A70 Aplastic anaemia 3A71 Anaemia due to chronic disease 3A72 Sideroblastic anaemia 3A73 Congenital dyserythropoietic anaemia 3A90 Anaemia due to acute disease 3A91 Congenital methaemoglobinaemia 3A92 Hereditary methaemoglobinaemia 3A93 Acquired methaemoglobinaemia 3A94 Acute posthaemorrhagic anaemia 3A9Y Other specified anaemias or erythrocyte disorders 3A9Z Anaemias or other erythrocyte disorders, unspecified 3A00 Iron deficiency anaemia 3A01 Megaloblastic anaemia due to vitamin B12 deficiency 3A02 Folate deficiency anaemia 3A03 Certain nutritional or metabolic anaemias 3A0Z Nutritional or metabolic anaemias, unspecified 3A4Z Haemolytic anaemias, unspecified 3A50.0 Alpha thalassaemia 3A50.1 Alpha thalassaemia related syndromes 3A50.2 Beta thalassaemia 3A50.3 Delta, delta-beta or gamma-delta-beta thalassaemia 3A50.4 Hereditary persistence of fetal haemoglobin 3A50.Y Other specified thalassaemias 3A50.Z Thalassaemias, unspecified 3A51.0 Sickle cell trait 3A51.1 Sickle cell disease without crisis 3A51.2 Sickle cell disease with crisis 3A51.3 Compound heterozygous sickling disorders without crisis 3A51.4 Compound heterozygous sickling disorders with crisis 3A51.5 Haemoglobin C disease 3A51.6 Haemoglobin D disease 3A51.7 High affinity haemoglobin 3A51.8 Low affinity haemoglobin 3A51.9 Haemoglobin O disease 3A51.A Haemoglobin E disease 3A51.B Haemoglobin C/beta thalassaemia compound heterozygosity 3A51.Y Other specified sickle cell disorders or other haemoglobinopathies 3A51.Z Sickle cell disorders or other haemoglobinopathies, unspecified 3A60 Congenital pure red cell aplasia 3A61 Acquired pure red cell aplasia 3A6Z Pure red cell aplasia, unspecified 3A70.0 Congenital aplastic anaemia 3A70.1 Acquired aplastic anaemias 3A70.Z Aplastic anaemia, unspecified 3A71.0 Anaemia in neoplastic disease 3A71.1 Anaemia in chronic infectious diseases 3A71.2 Anaemia in chronic kidney disease 3A71.Y Anaemia due to other specified chronic disease 3A71.Z Anaemia due to chronic disease, unspecified 3A72.0 Congenital sideroblastic anaemias 3A72.1 Acquired sideroblastic anaemias 3A72.Z Sideroblastic anaemia, unspecified 3A80 Congenital polycythaemia 3A81 Acquired polycythaemia 3A8Z Polycythaemia, unspecified 3A00.0 Acquired iron deficiency anaemia due to blood loss 3A00.1 Acquired iron deficiency anaemia due to low intake 3A00.2 Acquired iron deficiency anaemia due to decreased absorption 3A00.3 Acquired iron deficiency anaemia due to increased requirement 3A00.Y Other specified iron deficiency anaemia 3A00.Z Iron deficiency anaemia, unspecified 3A01.0 Hereditary vitamin B12 deficiency anaemia 3A01.1 Neonatal vitamin B12 deficiency anaemia 3A01.2 Vitamin B12 deficiency anaemia due to low intake 3A01.3 Vitamin B12 deficiency anaemia due to intrinsic factor deficiency 3A01.4 Vitamin B12 deficiency anaemia due to intestinal disease 3A01.5 Drug-induced vitamin B12 deficiency anaemia 3A01.Y Other specified megaloblastic anaemia due to vitamin B12 deficiency 3A01.Z Megaloblastic anaemia due to vitamin B12 deficiency, unspecified 3A02.0 Hereditary folate deficiency anaemia 3A02.1 Folate deficiency anaemia due to low intake 3A02.2 Folate deficiency anaemia due to increased requirements 3A02.3 Folate deficiency anaemia due to decreased intestinal absorption 3A02.4 Drug-induced folate deficiency anaemia 3A02.Y Other specified folate deficiency anaemia 3A02.Z Folate deficiency anaemia, unspecified 3A03.0 Hereditary orotic aciduria 3A03.1 Protein deficiency anaemia 3A03.2 Scorbutic anaemia 3A03.3 Copper deficiency anaemia 3A03.4 Acquired other vitamin B deficiency anaemia 3A03.5 Acquired vitamin A deficiency anaemia 3A03.6 Acquired vitamin E deficiency anaemia 3A03.Y Other and unspecified nutritional or metabolic anaemia 3A10 Hereditary haemolytic anaemia 3A1Y Other specified congenital haemolytic anaemia 3A20 Acquired haemolytic anaemia, immune 3A21 Acquired haemolytic anaemia, non-immune 3A2Z Acquired haemolytic anaemia, unspecified 3A50.00 Mild alpha thalassaemia diseases 3A50.01 Thalassaemic alpha-chain variants 3A50.02 Haemoglobin H disease (– α/– – included) 3A50.03 Hemoglobin Bart's fetalis syndrome 3A50.0Y Other specified alpha thalassaemia 3A50.0Z Alpha thalassaemia, unspecified 3A60.0 Congenital non-inherited pure red cell aplasia 3A60.1 Hereditary pure red cell aplasia 3A60.Z Congenital pure red cell aplasia, unspecified 3A61.0 Acute acquired pure red cell aplasia 3A61.1 Chronic acquired pure red cell aplasia 3A61.Y Other specified acquired pure red cell aplasia 3A61.Z Acquired pure red cell aplasia, unspecified 3A70.10 Drug-induced aplastic anaemia 3A70.11 Aplastic anaemia due to other external agents 3A70.12 Idiopathic aplastic anaemia 3A70.1Y Other specified acquired aplastic anaemias 3A70.1Z Acquired aplastic anaemias, unspecified 3A72.00 Hereditary sideroblastic anaemias 3A72.01 Hereditary syndromic sideroblastic anaemia 3A72.0Y Other specified congenital sideroblastic anaemias 3A72.0Z Congenital sideroblastic anaemias, unspecified 3A80.0 Primary inherited erythrocytosis 3A80.Y Other specified congenital polycythaemia 3A80.Z Congenital polycythaemia, unspecified 3A81.0 Polycythaemia due to hypoxia, including high altitude 3A81.1 Polycythaemia due to over-transfusion or blood doping 3A81.2 Relative polycythaemia 3A81.Y Other specified acquired polycythaemia 3A81.Z Acquired polycythaemia, unspecified 3A00.01 Chronic posthaemorrhagic anaemia 3A00.0Z Acquired iron deficiency anaemia due to blood loss, unspecified 3A01.30 Pernicious anaemia 3A01.3Y Other specified vitamin B12 deficiency anaemia due to intrinsic factor deficiency 3A01.3Z Vitamin B12 deficiency anaemia due to intrinsic factor deficiency, unspecified 3A03.40 Acquired pyridoxine deficiency anaemia 3A03.41 Acquired riboflavin deficiency anaemia 3A03.42 Acquired thiamine deficiency anaemia 3A03.4Y Other specified acquired other vitamin B deficiency anaemia 3A10.0 Haemolytic anaemias due to hexose monophosphate shunt or glutathione metabolism anomalies 3A10.1 Haemolytic anaemia due to adenosine deaminase excess 3A10.2 Hereditary elliptocytosis 3A10.3 Familial pseudohyperkalaemia 3A10.Y Other specified hereditary haemolytic anaemia 3A10.Z Hereditary haemolytic anaemia, unspecified 3A20.0 Autoimmune haemolytic anaemia, warm type 3A20.1 Autoimmune haemolytic anaemia, cold type 3A20.2 Autoimmune haemolytic anaemia, mixed type, cold and warm 3A20.3 Paroxysmal cold haemoglobinuria 3A20.4 Alloimmune haemolytic anaemia 3A20.5 Evans syndrome 3A20.Y Other specified acquired haemolytic anaemia, immune 3A20.Z Acquired haemolytic anaemia, immune, unspecified 3A21.0 Paroxysmal nocturnal haemoglobinuria 3A21.1 Microangiopathic haemolytic anaemia 3A21.2 Haemolytic uraemic syndrome 3A21.Y Other specified acquired haemolytic anaemia, non-immune 3A21.Z Acquired haemolytic anaemia, non-immune, unspecified 3A10.00 Haemolytic anaemia due to glucose-6-phosphate dehydrogenase deficiency 3A10.0Y Other specified haemolytic anaemias due to hexose monophosphate shunt or glutathione metabolism anomalies 3A10.0Z Haemolytic anaemias due to hexose monophosphate shunt or glutathione metabolism anomalies, unspecified ME24 Clinical manifestations of the digestive system ME24.0 Digestive system abscess ME24.1 Digestive system fistula ME24.2 Digestive system obstruction ME24.3 Digestive system perforation ME24.4 Digestive system stenosis ME24.5 Digestive system ulcer ME24.6 Digestive system dilatation ME24.7 Digestive system incarceration ME24.8 Digestive system strangulation or gangrene ME24.9 Gastrointestinal bleeding ME24.A Other digestive system haemorrhage, not elsewhere classified ME24.Y Other specified clinical manifestations of the digestive system ME24.30 Perforation of small intestine ME24.31 Perforation of large intestine ME24.35 Perforation of gallbladder or bile ducts ME24.3Y Digestive system perforation of other specified site ME24.3Z Digestive system perforation of unspecified site ME24.90 Acute gastrointestinal bleeding, not elsewhere classified ME24.91 Chronic gastrointestinal bleeding, not elsewhere classified ME24.9Z Gastrointestinal bleeding, unspecified ME24.A0 Obscure gastrointestinal bleeding ME24.A1 Haemorrhage of anus or rectum ME24.A2 Oesophageal haemorrhage ME24.A3 Haematochezia ME24.A4 Melaena ME24.A5 Haematemesis ME24.A6 Positive occult blood in stool
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