Code
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| Description
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228
|
|---|---|
D72825
|
Bandemia
|
D72828
|
Other elevated white blood cell count
|
D72829
|
Elevated white blood cell count, unspecified
|
D7289
|
Other specified disorders of white blood cells
|
D729
|
Disorder of white blood cells, unspecified
|
D730
|
Hyposplenism
|
D731
|
Hypersplenism
|
D732
|
Chronic congestive splenomegaly
|
D733
|
Abscess of spleen
|
D734
|
Cyst of spleen
|
D735
|
Infarction of spleen
|
D7381
|
Neutropenic splenomegaly
|
D7389
|
Other diseases of spleen
|
D739
|
Disease of spleen, unspecified
|
D740
|
Congenital methemoglobinemia
|
D748
|
Other methemoglobinemias
|
D749
|
Methemoglobinemia, unspecified
|
D750
|
Familial erythrocytosis
|
D751
|
Secondary polycythemia
|
D7581
|
Myelofibrosis
|
D7582
|
Heparin induced thrombocytopenia (HIT)
|
D75838
|
Other thrombocytosis
|
D75839
|
Thrombocytosis, unspecified
|
D7589
|
Other specified diseases of blood and blood-forming organs
|
D759
|
Disease of blood and blood-forming organs, unspecified
|
D75A
|
Glucose-6-phosphate dehydrogenase (G6PD) deficiency without anemia
|
D761
|
Hemophagocytic lymphohistiocytosis
|
D762
|
Hemophagocytic syndrome, infection-associated
|
D763
|
Other histiocytosis syndromes
|
D77
|
Other disorders of blood and blood-forming organs in diseases classified elsewhere
|
D7801
|
Intraoperative hemorrhage and hematoma of the spleen complicating a procedure on the spleen
|
D7802
|
Intraoperative hemorrhage and hematoma of the spleen complicating other procedure
|
D7811
|
Accidental puncture and laceration of the spleen during a procedure on the spleen
|
D7812
|
Accidental puncture and laceration of the spleen during other procedure
|
D7821
|
Postprocedural hemorrhage of the spleen following a procedure on the spleen
|
D7822
|
Postprocedural hemorrhage of the spleen following other procedure
|
D7831
|
Postprocedural hematoma of the spleen following a procedure on the spleen
|
D7832
|
Postprocedural hematoma of the spleen following other procedure
|
D7833
|
Postprocedural seroma of the spleen following a procedure on the spleen
|
D7834
|
Postprocedural seroma of the spleen following other procedure
|
D7881
|
Other intraoperative complications of the spleen
|
D7889
|
Other postprocedural complications of the spleen
|
D800
|
Hereditary hypogammaglobulinemia
|
D801
|
Nonfamilial hypogammaglobulinemia
|
D802
|
Selective deficiency of immunoglobulin A [IgA]
|
D803
|
Selective deficiency of immunoglobulin G [IgG] subclasses
|
D804
|
Selective deficiency of immunoglobulin M [IgM]
|
D805
|
Immunodeficiency with increased immunoglobulin M [IgM]
|
D806
|
Antibody deficiency with near-normal immunoglobulins or with hyperimmunoglobulinemia
|
D807
|
Transient hypogammaglobulinemia of infancy
|
D808
|
Other immunodeficiencies with predominantly antibody defects
|
D809
|
Immunodeficiency with predominantly antibody defects, unspecified
|
D810
|
Severe combined immunodeficiency [SCID] with reticular dysgenesis
|
D811
|
Severe combined immunodeficiency [SCID] with low T- and B-cell numbers
|
D812
|
Severe combined immunodeficiency [SCID] with low or normal B-cell numbers
|
D8130
|
Adenosine deaminase deficiency, unspecified
|
D8131
|
Severe combined immunodeficiency due to adenosine deaminase deficiency
|
D8132
|
Adenosine deaminase 2 deficiency
|
D8139
|
Other adenosine deaminase deficiency
|
D814
|
Nezelof's syndrome
|
D815
|
Purine nucleoside phosphorylase [PNP] deficiency
|
D816
|
Major histocompatibility complex class I deficiency
|
D817
|
Major histocompatibility complex class II deficiency
|
D81810
|
Biotinidase deficiency
|
D81818
|
Other biotin-dependent carboxylase deficiency
|
D81819
|
Biotin-dependent carboxylase deficiency, unspecified
|
D8189
|
Other combined immunodeficiencies
|
D819
|
Combined immunodeficiency, unspecified
|
D820
|
Wiskott-Aldrich syndrome
|
D821
|
Di George's syndrome
|
D822
|
Immunodeficiency with short-limbed stature
|
D823
|
Immunodeficiency following hereditary defective response to Epstein-Barr virus
|
D824
|
Hyperimmunoglobulin E [IgE] syndrome
|
D828
|
Immunodeficiency associated with other specified major defects
|
D829
|
Immunodeficiency associated with major defect, unspecified
|
D830
|
Common variable immunodeficiency with predominant abnormalities of B-cell numbers and function
|
D831
|
Common variable immunodeficiency with predominant immunoregulatory T-cell disorders
|
D832
|
Common variable immunodeficiency with autoantibodies to B- or T-cells
|
D838
|
Other common variable immunodeficiencies
|
D839
|
Common variable immunodeficiency, unspecified
|
D840
|
Lymphocyte function antigen-1 [LFA-1] defect
|
D841
|
Defects in the complement system
|
D8481
|
Immunodeficiency due to conditions classified elsewhere
|
D84821
|
Immunodeficiency due to drugs
|
D84822
|
Immunodeficiency due to external causes
|
D8489
|
Other immunodeficiencies
|
D849
|
Immunodeficiency, unspecified
|
D860
|
Sarcoidosis of lung
|
D861
|
Sarcoidosis of lymph nodes
|
D862
|
Sarcoidosis of lung with sarcoidosis of lymph nodes
|
D863
|
Sarcoidosis of skin
|
D8681
|
Sarcoid meningitis
|
D8682
|
Multiple cranial nerve palsies in sarcoidosis
|
D8683
|
Sarcoid iridocyclitis
|
D8684
|
Sarcoid pyelonephritis
|
D8685
|
Sarcoid myocarditis
|
D8686
|
Sarcoid arthropathy
|
D8687
|
Sarcoid myositis
|
D8689
|
Sarcoidosis of other sites
|
D869
|
Sarcoidosis, unspecified
|
Subsets and Splits
Diabetes Codes E10-E14
The query retrieves and sorts records with "Code" values between 'E10' and 'E14', offering a basic filter of the dataset but not providing significant analytical insights.