Códigos SUNAT de diagnoses of diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism
La familia 85320000 reúne 22 clases y 88 códigos de producto. Busca la clase de tu producto y usa el código de 8 dígitos en la línea de tu factura o boleta. Si no lo ves claro, usa el buscador por nombre.
85321500 Diagnoses of endocrine, nutritional and metabolic diseases
- 85321501Diagnoses of iron deficiency anaemia
- 85321502Diagnoses of vitamin b 12 deficiency anaemia
- 85321503Diagnosis of vitamin b 12 deficiency anaemia due to intrinsic factor deficiency
- 85321504Diagnosis of vitamin b 12 deficiency anaemia due to selective vitamin b 12 malabsorption with proteinuria
- 85321505Diagnosis of transcobalamin ii deficiency
- 85321506Diagnoses of folate deficiency anaemia
- 85321507Diagnosis of dietary folate deficiency anaemia
- 85321508Diagnosis of drug-induced folate deficiency anaemia
85321600 Diagnoses of sickle-cell disorders
- 85321601Diagnosis of sickle-cell anaemia with crisis
- 85321602Diagnosis of sickle-cell anaemia without crisis
- 85321603Diagnosis of double heterozygous sickling disorders
- 85321604Diagnosis of sickle-cell trait
85321700 Diagnoses of hereditary haemolytic anaemias
- 85321701Diagnosis of hereditary spherocytosis
- 85321702Diagnosis of hereditary elliptocytosis
85321800 Diagnoses of acquired haemolytic anaemia
- 85321801Diagnosis of drug-induced autoimmune haemolytic anaemia
- 85321802Diagnosis of drug-induced nonautoimmune haemolytic anaemia
- 85321803Diagnosis of haemolytic-uraemic syndrome
- 85321804Diagnosis of paroxysmal nocturnal haemoglobinuria or marchiafava-micheli
85321900 Diagnoses of acquired pure red cell aplasia or erythroblastopenia
- 85321901Diagnosis of chronic acquired pure red cell aplasia
- 85321902Diagnosis of transient acquired pure red cell aplasia
85322000 Diagnoses of aplastic anaemias
- 85322001Diagnosis of constitutional aplastic anaemia
- 85322002Diagnosis of drug-induced aplastic anaemia
- 85322003Diagnosis of idiopathic aplastic anaemia
- 85322004Diagnosis of acute posthaemorrhagic anaemia
85322100 Diagnoses of neoplastic, sideroblastic, or dyserythropoietic anaemia diseases
- 85322101Diagnosis of anaemia in neoplastic disease
- 85322102Diagnosis of hereditary sideroblastic anaemia
- 85322103Diagnosis of secondary sideroblastic anaemia due to disease
- 85322104Diagnosis of secondary sideroblastic anaemia due to drugs and toxins
- 85322105Diagnosis of congenital dyserythropoietic anaemia
85322200 Diagnoses of hereditary factor deficiencies
- 85322201Diagnosis of hereditary factor viii deficiency
- 85322202Diagnosis of hereditary factor ix deficiency
85322300 Diagnoses of peripheral coagulation defects
- 85322301Diagnosis of von willebrand disease
- 85322302Diagnosis of hereditary factor xi deficiency
- 85322303Diagnosis of haemorrhagic disorder due to circulating anticoagulants
- 85322304Diagnosis of acquired coagulation factor deficiency
- 85322305Diagnosis of primary thrombophilia
85322400 Diagnoses of purpura and peripheral haemorrhagic conditions
- 85322401Diagnosis of allergic purpura
- 85322402Diagnosis of qualitative platelet defects
- 85322403Diagnosis of idiopathic thrombocytopenic purpura
- 85322404Diagnosis of secondary thrombocytopenia
85322500 Diagnoses of intravascular coagulation or arganulocytosis or functional disorders of polymorhponuclear neutrophils
- 85322501Diagnosis of disseminated intravascular coagulation or defibrination syndrome
- 85322502Diagnosis of agranulocytosis
- 85322503Diagnosis of functional disorders of polymorphonuclear neutrophils
85322600 Diagnoses of peripheral disorders of white blood cells
- 85322601Diagnosis of genetic anomalies of leukocytes
- 85322602Diagnosis of eosinophilia
85322700 Diagnoses of diseases of spleen
- 85322701Diagnosis of hyposplenism
- 85322702Diagnosis of hypersplenism
- 85322703Diagnosis of chronic congestive splenomegaly
- 85322704Diagnosis of abscess of spleen
- 85322705Diagnosis of cyst of spleen
- 85322706Diagnosis of infarction of spleen
85322800 Diagnoses of peripheral diseases of blood and blood-forming organs
- 85322801Diagnosis of familial erythrocytosis
- 85322802Diagnosis of secondary polycythaemia
85322900 Diagnoses of specified diseases with participation of lymphoreticular and reticulohistiocytic tissue
- 85322901Diagnosis of haemophagocytic lymphohistiocytosis
- 85322902Diagnosis of haemophagocytic syndrome, infection-associated
85323000 Diagnoses of immunodeficiency with predominantly antibody defects
- 85323001Diagnosis of hereditary hypogammaglobulinaemia
- 85323002Diagnosis of nonfamilial hypogammaglobulinaemia
- 85323003Diagnosis of selective deficiency of immunoglobulin a or iga
- 85323004Diagnosis of selective deficiency of immunoglobulin g or igg subclasses
- 85323005Diagnosis of selective deficiency of immunoglobulin m or igm
- 85323006Diagnosis of immunodeficiency with increased immunoglobulin m or igm
- 85323007Diagnosis of antibody deficiency with near-normal immunoglobulins or with hyperimmunoglobulinaemia
- 85323008Diagnosis of transient hypogammaglobulinaemia of infancy
85323100 Diagnoses of combined immunodeficiencies
- 85323101Diagnosis of severe combined immunodeficiency or scid with reticular dysgenesis
- 85323102Diagnosis of severe combined immunodeficiency or scid with low t- and b-cell numbers
- 85323103Diagnosis of severe combined immunodeficiency or scid with low or normal b-cell numbers
- 85323104Diagnosis of adenosine deaminase or ada deficiency
- 85323105Diagnosis of nezelof syndrome
- 85323106Diagnosis of purine nucleoside phosphorylase or pnp deficiency
- 85323107Diagnosis of major histocompatibility complex class i deficiency
- 85323108Diagnosis of major histocompatibility complex class ii deficiency
85323200 Diagnoses of immunodeficiency associated with peripheral major defects
- 85323201Diagnosis of wiskott-aldrich syndrome
- 85323202Diagnosis of di george syndrome
- 85323203Diagnosis of immunodeficiency with short-limbed stature
- 85323204Diagnosis of immunodeficiency following hereditary defective response to epstein-barr virus
- 85323205Diagnosis of hyperimmunoglobulin e or ige syndrome
85323300 Diagnoses of common variable immunodeficiency
- 85323301Diagnosis of common variable immunodeficiency with predominant abnormalities of b-cell numbers and function
- 85323302Diagnosis of common variable immunodeficiency with predominant immunoregulatory t-cell disorders
- 85323303Diagnosis of common variable immunodeficiency with autoantibodies to b- or t-cells
85323400 Diagnoses of lymphocyte or complement system immunodeficiencies
- 85323401Diagnosis of lymphocyte function antigen-1 or lfa-1 defect
- 85323402Diagnosis of defects in the complement system
85323500 Diagnoses of sarcoidosis
- 85323501Diagnosis of sarcoidosis of lung
- 85323502Diagnosis of sarcoidosis of lymph nodes
- 85323503Diagnosis of sarcoidosis of lung with sarcoidosis of lymph nodes
- 85323504Diagnosis of sarcoidosis of skin
85323600 Diagnoses of polyclonal hypergammaglobulinaemia or cryoglobulinaemia or immune reconstitution syndrome
- 85323601Diagnosis of polyclonal hypergammaglobulinaemia
- 85323602Diagnosis of cryoglobulinaemia
- 85323603Diagnosis of immune reconstitution syndrome