icd10Code
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Disease
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228
D73.81
Neutropenic splenomegaly
D73.89
Other diseases of spleen
D73.9
Disease of spleen unspecified
D74.0
Congenital methemoglobinemia
D74.8
Other methemoglobinemias
D74.9
Methemoglobinemia unspecified
D75.0
Familial erythrocytosis
D75.1
Secondary polycythemia
D75.8
Other specified diseases of blood and blood-forming organs
D75.81
Myelofibrosis
D75.82
Heparin induced thrombocytopenia (HIT)
D75.89
Other specified diseases of blood and blood-forming organs
D75.9
Disease of blood and blood-forming organs unspecified
D76.1
Hemophagocytic lymphohistiocytosis
D76.2
Hemophagocytic syndrome infection-associated
D76.3
Other histiocytosis syndromes
D78.0
Intraoperative hemorrhage and hematoma of the spleen complicating a procedure
D78.01
Intraoperative hemorrhage and hematoma of the spleen complicating a procedure on the spleen
D78.02
Intraoperative hemorrhage and hematoma of the spleen complicating other procedure
D78.1
Accidental puncture and laceration of the spleen during a procedure
D78.11
Accidental puncture and laceration of the spleen during a procedure on the spleen
D78.12
Accidental puncture and laceration of the spleen during other procedure
D78.2
Postprocedural hemorrhage of the spleen following a procedure
D78.21
Postprocedural hemorrhage of the spleen following a procedure on the spleen
D78.22
Postprocedural hemorrhage of the spleen following other procedure
D78.3
Postprocedural hematoma and seroma of the spleen following a procedure
D78.31
Postprocedural hematoma of the spleen following a procedure on the spleen
D78.32
Postprocedural hematoma of the spleen following other procedure
D78.33
Postprocedural seroma of the spleen following a procedure on the spleen
D78.34
Postprocedural seroma of the spleen following other procedure
D78.8
Other intraoperative and postprocedural complications of the spleen
D78.81
Other intraoperative complications of the spleen
D78.89
Other postprocedural complications of the spleen
D80.0
Hereditary hypogammaglobulinemia
D80.1
Nonfamilial hypogammaglobulinemia
D80.2
Selective deficiency of immunoglobulin A [IgA]
D80.3
Selective deficiency of immunoglobulin G [IgG] subclasses
D80.4
Selective deficiency of immunoglobulin M [IgM]
D80.5
Immunodeficiency with increased immunoglobulin M [IgM]
D80.6
Antibody deficiency with near-normal immunoglobulins or with hyperimmunoglobulinemia
D80.7
Transient hypogammaglobulinemia of infancy
D80.8
Other immunodeficiencies with predominantly antibody defects
D80.9
Immunodeficiency with predominantly antibody defects unspecified
D81.0
Severe combined immunodeficiency [SCID] with reticular dysgenesis
D81.1
Severe combined immunodeficiency [SCID] with low T- and B-cell numbers
D81.2
Severe combined immunodeficiency [SCID] with low or normal B-cell numbers
D81.3
Adenosine deaminase [ADA] deficiency
D81.4
Nezelof's syndrome
D81.5
Purine nucleoside phosphorylase [PNP] deficiency
D81.6
Major histocompatibility complex class I deficiency
D81.7
Major histocompatibility complex class II deficiency
D81.8
Other combined immunodeficiencies
D81.81
Biotin-dependent carboxylase deficiency
D81.810
Biotinidase deficiency
D81.818
Other biotin-dependent carboxylase deficiency
D81.819
Biotin-dependent carboxylase deficiency unspecified
D81.89
Other combined immunodeficiencies
D81.9
Combined immunodeficiency unspecified
D82.0
Wiskott-Aldrich syndrome
D82.1
Di George's syndrome
D82.2
Immunodeficiency with short-limbed stature
D82.3
Immunodeficiency following hereditary defective response to Epstein-Barr virus
D82.4
Hyperimmunoglobulin E [IgE] syndrome
D82.8
Immunodeficiency associated with other specified major defects
D82.9
Immunodeficiency associated with major defect unspecified
D83.0
Common variable immunodeficiency with predominant abnormalities of B-cell numbers and function
D83.1
Common variable immunodeficiency with predominant immunoregulatory T-cell disorders
D83.2
Common variable immunodeficiency with autoantibodies to B- or T-cells
D83.8
Other common variable immunodeficiencies
D83.9
Common variable immunodeficiency unspecified
D84.0
Lymphocyte function antigen-1 [LFA-1] defect
D84.1
Defects in the complement system
D84.8
Other specified immunodeficiencies
D84.9
Immunodeficiency unspecified
D86.0
Sarcoidosis of lung
D86.1
Sarcoidosis of lymph nodes
D86.2
Sarcoidosis of lung with sarcoidosis of lymph nodes
D86.3
Sarcoidosis of skin
D86.8
Sarcoidosis of other sites
D86.81
Sarcoid meningitis
D86.82
Multiple cranial nerve palsies in sarcoidosis
D86.83
Sarcoid iridocyclitis
D86.84
Sarcoid pyelonephritis
D86.85
Sarcoid myocarditis
D86.86
Sarcoid arthropathy
D86.87
Sarcoid myositis
D86.89
Sarcoidosis of other sites
D86.9
Sarcoidosis unspecified
D89.0
Polyclonal hypergammaglobulinemia
D89.1
Cryoglobulinemia
D89.2
Hypergammaglobulinemia unspecified
D89.3
Immune reconstitution syndrome
D89.4
Mast cell activation syndrome and related disorders
D89.40
Mast cell activation unspecified
D89.41
Monoclonal mast cell activation syndrome
D89.42
Idiopathic mast cell activation syndrome
D89.43
Secondary mast cell activation
D89.49
Other mast cell activation disorder
D89.8
Other specified disorders involving the immune mechanism not elsewhere classified
D89.81
Graft-versus-host disease