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1C62.2 HIV disease clinical stage 3 without mention of tuberculosis or malaria International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01 postcoordination Add Stem and/or Extension codes to form a cluster code which adds detail to the condition.
Has manifestation - multiple selections are allowed [select] MG30 Chronic pain – MG30.0 Chronic primary pain – MG30.1 Chronic cancer related pain – MG30.2 Chronic postsurgical or post traumatic pain – MG30.3 Chronic secondary musculoskeletal pain – MG30.4 Chronic secondary visceral pain – MG30.5 Chronic neuropathic pain – MG30.6 Chronic secondary headache or orofacial pain – MG30.Y Other specified chronic pain – MG30.Z Chronic pain, unspecified –– MG30.00 Chronic primary visceral pain –– MG30.01 Chronic widespread pain –– MG30.02 Chronic primary musculoskeletal pain –– MG30.03 Chronic primary headache or orofacial pain –– MG30.04 Complex regional pain syndrome –– MG30.0Y Other specified chronic primary pain –– MG30.0Z Chronic primary pain, unspecified –– MG30.10 Chronic cancer pain –– MG30.11 Chronic post cancer treatment pain –– MG30.1Y Other specified chronic cancer related pain –– MG30.1Z Chronic cancer related pain, unspecified –– MG30.20 Chronic post traumatic pain –– MG30.21 Chronic postsurgical pain –– MG30.2Y Other specified chronic postsurgical or post traumatic pain –– MG30.2Z Chronic postsurgical or post traumatic pain, unspecified –– MG30.30 Chronic secondary musculoskeletal pain from persistent inflammation –– MG30.31 Chronic secondary musculoskeletal pain associated with structural changes –– MG30.32 Chronic secondary musculoskeletal pain due to disease of the nervous system –– MG30.3Y Other specified chronic secondary musculoskeletal pain –– MG30.3Z Chronic secondary musculoskeletal pain, unspecified –– MG30.40 Chronic visceral pain from mechanical factors –– MG30.41 Chronic visceral pain from vascular mechanisms –– MG30.42 Chronic visceral pain from persistent inflammation –– MG30.4Y Other specified chronic secondary visceral pain –– MG30.4Z Chronic secondary visceral pain, unspecified –– MG30.50 Chronic central neuropathic pain –– MG30.51 Chronic peripheral neuropathic pain –– MG30.5Y Other specified chronic neuropathic pain –– MG30.5Z Chronic neuropathic pain, unspecified –– MG30.61 Chronic dental pain –– MG30.62 Chronic neuropathic orofacial pain –– MG30.63 Headache or orofacial pain associated with chronic secondary temporomandibular disorders –– MG30.64 Chronic headache or orofacial pain associated with disorders of homoeostasis or their nonpharmacological treatment –– MG30.65 Chronic headache or orofacial pain associated with cranial or cervical vascular disorder –– MG30.66 Chronic headache or orofacial pain associated with non-vascular intracranial disorder –– MG30.67 Chronic headache associated with a substance or its withdrawal –– MG30.6Y Other specified chronic secondary headache or orofacial pain –– MG30.6Z Chronic secondary headache or orofacial pain, unspecified Associated with - multiple selections are allowed [select] 1C8E Viral meningitis, not elsewhere classified – 1C8E.1 Enteroviral meningitis – 1C8E.2 Meningitis due to adenovirus – 1C8E.Y Other specified viral meningitis, not elsewhere classified – 1C8E.Z Viral meningitis, unspecified – 1F23.0 Candidosis of lips or oral mucous membranes – 3A00 Iron deficiency anaemia –– 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 ––– 3A00.01 Chronic posthaemorrhagic anaemia ––– 3A00.0Z Acquired iron deficiency anaemia due to blood loss, unspecified – 3A01 Megaloblastic anaemia due to vitamin B12 deficiency –– 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 ––– 3A01.30 Pernicious anaemia ––– 3A01.3Y Other specified vitamin B12 deficiency anaemia due to intrinsic factor deficiency – 3A02 Folate deficiency anaemia –– 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 Other nutritional or metabolic anaemias –– 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 ––– 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 Hereditary haemolytic 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 –––– 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 –– 3A1Y Other specified congenital haemolytic anaemia –– 3A20 Acquired haemolytic anaemia, immune ––– 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 –– 3A21 Acquired haemolytic anaemia, non-immune ––– 3A21.0 Paroxysmal nocturnal haemoglobinuria ––– 3A21.1 Microangiopathic haemolytic anaemia ––– 3A21.2 Haemolytic uraemic syndrome ––– 3A21.Y Other specified acquired haemolytic anaemia, non-immune –– 3A2Z Acquired haemolytic anaemia, unspecified – 3A4Z Haemolytic anaemias, unspecified 3A50 Thalassaemias – 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 –– 3A50.00 Mild alpha thalassaemia diseases –– 3A50.01 Thalassaemic alpha-chain variants –– 3A50.02 Haemoglobin H disease (– α/– – included) –– 3A50.03 Homozygous or compound heterozygous alpha0 thalassaemia –– 3A50.0Y Other specified alpha thalassaemia –– 3A50.0Z Alpha thalassaemia, unspecified 3A51 Sickle cell disorders or other haemoglobinopathies – 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 –– 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 Acquired pure red cell aplasia –– 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 – 3A6Z Pure red cell aplasia, unspecified 3A70 Aplastic anaemia – 3A70.0 Congenital aplastic anaemia – 3A70.1 Acquired aplastic anaemias – 3A70.Z Aplastic anaemia, 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 3A71 Anaemia due to chronic disease – 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 Sideroblastic anaemia – 3A72.0 Congenital sideroblastic anaemias – 3A72.1 Acquired sideroblastic anaemias – 3A72.Z Sideroblastic anaemia, 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 3A73 Congenital dyserythropoietic anaemia – 3A80 Congenital polycythaemia –– 3A80.0 Primary inherited erythrocytosis –– 3A80.Y Other specified congenital polycythaemia –– 3A80.Z Congenital polycythaemia, unspecified – 3A81 Acquired polycythaemia –– 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 – 3A8Z Polycythaemia, unspecified 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 3B64 Thrombocytopenia – 3B64.0 Congenital thrombocytopenia – 3B64.1 Acquired thrombocytopenia – 3B64.Z Thrombocytopenia, unspecified –– 3B64.00 Congenital non-inherited thrombocytopenia –– 3B64.01 Hereditary thrombocytopenia –– 3B64.0Z Congenital thrombocytopenia, unspecified –– 3B64.10 Immune thrombocytopenic purpura –– 3B64.11 Secondary thrombocytopenic purpura –– 3B64.12 Drug-induced thrombocytopenic purpura –– 3B64.13 Alloimmune thrombocytopenia –– 3B64.14 Thrombotic thrombocytopenic purpura –– 3B64.1Y Other specified acquired thrombocytopenia 4B00 Disorders of neutrophil number – 4B00.0 Neutropaenia – 4B00.1 Neutrophilia – 4B00.Y Other specified disorders of neutrophil number –– 4B00.00 Constitutional neutropaenia –– 4B00.01 Acquired neutropaenia –– 4B00.0Z Neutropaenia, unspecified –– 4B00.10 Constitutional neutrophilia –– 4B00.11 Acquired neutrophilia –– 4B00.1Z Neutrophilia, unspecified – CA40.0 Bacterial pneumonia –– CA40.00 Pneumonia due to Chlamydophila pneumoniae –– CA40.01 Pneumonia due to Escherichia coli –– CA40.02 Pneumonia due to Haemophilus influenzae –– CA40.03 Pneumonia due to Klebsiella pneumoniae –– CA40.04 Pneumonia due to Mycoplasma pneumoniae –– CA40.05 Pneumonia due to Pseudomonas aeruginosa –– CA40.06 Pneumonia due to Staphylococcus –– CA40.07 Pneumonia due to Streptococcus pneumoniae –– CA40.08 Pneumonia due to beta-haemolytic streptococcus –– CA40.0Y Pneumonia due to other specified bacteria –– CA40.0Z Bacterial pneumonia, unspecified CA44 Pyothorax –– DA01.01 Hairy leukoplakia – DA0C.3 Necrotising periodontal diseases –– DA0C.30 Necrotising ulcerative periodontitis –– DA0C.31 Noma –– DA0C.3Y Other specified necrotising periodontal diseases –– DA0C.3Z Necrotising periodontal diseases, unspecified – FA10 Direct infections of joint –– FA10.0 Bacterial infection of joint –– FA10.1 Viral infection of joint –– FA10.2 Fungal infection of joint –– FA10.Z Direct infections of joint, unspecified – FA11 Reactive arthropathies –– FA11.0 Arthropathy following intestinal bypass –– FA11.1 Arthropathy following vaccination –– FA11.2 Arthropathy following genitourinary infection –– FA11.Y Other specified reactive arthropathies –– FA11.Z Reactive arthropathies, unspecified – FA12 Postinfectious arthropathies –– FA12.0 Bacterial postinfectious arthropathy –– FA12.1 Viral postinfectious arthropathies –– FA12.2 Fungal postinfectious arthropathies –– FA12.3 Parasitic postinfectious arthropathies –– FA12.Y Other specified postinfectious arthropathies –– FA12.Z Postinfectious arthropathies, unspecified – FA13 Infectious spondyloarthritis – FA1Y Other specified infection related arthropathies – FA1Z Infection related arthropathies, unspecified – FB30 Infectious myositis ––– ME05.1 Diarrhoea – MG26 Fever of other or unknown origin –– MG53.0 Antiretroviral therapy resistant Human immunodeficiency virus
synonyms HIV disease clinical stage 3 without mention of tuberculosis or malaria HIV disease clinical stage 3 without tuberculosis or malaria HIV disease resulting in Pneumocystis jirovecii pneumonia HIV - [human immunodeficiency virus] disease resulting in Pneumocystis carinii pneumonia pneumocystosis resulting from HIV - [human immunodeficiency virus] disease Human immunodeficiency virus disease associated with haematological or immunological abnormalities abnormal immunological findings resulting from HIV - [human immunodeficiency virus] Human immunodeficiency virus disease associated with lymphoid interstitial pneumonitis HIV - [human immunodeficiency virus] disease resulting in interstitial lymphatic pneumonitis Human immunodeficiency virus disease enteritis AIDS - [acquired immunodeficiency syndrome] enteropathy Gastritis due to human immunodeficiency virus disease Myelitis due to Human immunodeficiency virus Myelitis due to HIV - [human immunodeficiency virus] Meningitis due to human immunodeficiency virus HIV disease resulting in candidosis classified elsewhere candida infection resulting from HIV - [human immunodeficiency virus] HIV - [human immunodeficiency virus] disease resulting in candidiasis HIV disease resulting in cytomegaloviral disease cytomegaloviral disease resulting from HIV - [human immunodeficiency virus]
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