ICD-10-CM/PCS MS-DRG v36.0 Definitions Manual
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MDC 16 Diseases & Disorders of Blood, Blood Forming Organs, Immunologic Disorders
Reticuloendothelial and Immunity Disorders
MCC CC DRG
Yes n/a 814
No Yes 815
No No 816

DRG 814 RETICULOENDOTHELIAL AND IMMUNITY DISORDERS WITH MCC

DRG 815 RETICULOENDOTHELIAL AND IMMUNITY DISORDERS WITH CC

DRG 816 RETICULOENDOTHELIAL AND IMMUNITY DISORDERS WITHOUT CC/MCC

PRINCIPAL DIAGNOSIS

A182Tuberculous peripheral lymphadenopathy
A1885Tuberculosis of spleen
A281Cat-scratch disease
D150Benign neoplasm of thymus
D181Lymphangioma, any site
D360Benign neoplasm of lymph nodes
D3A091Benign carcinoid tumor of the thymus
D472Monoclonal gammopathy
D473Essential (hemorrhagic) thrombocythemia
D474Osteomyelofibrosis
D68312Antiphospholipid antibody with hemorrhagic disorder
D6851Activated protein C resistance
D6852Prothrombin gene mutation
D6859Other primary thrombophilia
D6861Antiphospholipid syndrome
D6862Lupus anticoagulant syndrome
D6869Other thrombophilia
D721Eosinophilia
D72810Lymphocytopenia
D72818Other decreased white blood cell count
D72819Decreased white blood cell count, unspecified
D72820Lymphocytosis (symptomatic)
D72821Monocytosis (symptomatic)
D72822Plasmacytosis
D72823Leukemoid reaction
D72824Basophilia
D72825Bandemia
D72828Other elevated white blood cell count
D72829Elevated white blood cell count, unspecified
D7289Other specified disorders of white blood cells
D729Disorder of white blood cells, unspecified
D730Hyposplenism
D731Hypersplenism
D732Chronic congestive splenomegaly
D733Abscess of spleen
D734Cyst of spleen
D735Infarction of spleen
D7381Neutropenic splenomegaly
D7389Other diseases of spleen
D739Disease of spleen, unspecified
D750Familial erythrocytosis
D751Secondary polycythemia
D7589Other specified diseases of blood and blood-forming organs
D759Disease of blood and blood-forming organs, unspecified
D761Hemophagocytic lymphohistiocytosis
D762Hemophagocytic syndrome, infection-associated
D763Other histiocytosis syndromes
D77Other disorders of blood and blood-forming organs in diseases classified elsewhere
D800Hereditary hypogammaglobulinemia
D801Nonfamilial hypogammaglobulinemia
D802Selective deficiency of immunoglobulin A [IgA]
D803Selective deficiency of immunoglobulin G [IgG] subclasses
D804Selective deficiency of immunoglobulin M [IgM]
D805Immunodeficiency with increased immunoglobulin M [IgM]
D807Transient hypogammaglobulinemia of infancy
D822Immunodeficiency with short-limbed stature
D823Immunodeficiency following hereditary defective response to Epstein-Barr virus
D824Hyperimmunoglobulin E [IgE] syndrome
D828Immunodeficiency associated with other specified major defects
D829Immunodeficiency associated with major defect, unspecified
D830Common variable immunodeficiency with predominant abnormalities of B-cell numbers and function
D831Common variable immunodeficiency with predominant immunoregulatory T-cell disorders
D832Common variable immunodeficiency with autoantibodies to B- or T-cells
D838Other common variable immunodeficiencies
D839Common variable immunodeficiency, unspecified
D840Lymphocyte function antigen-1 [LFA-1] defect
D848Other specified immunodeficiencies
D849Immunodeficiency, unspecified
D890Polyclonal hypergammaglobulinemia
D892Hypergammaglobulinemia, unspecified
D893Immune reconstitution syndrome
D8940Mast cell activation, unspecified
D8941Monoclonal mast cell activation syndrome
D8942Idiopathic mast cell activation syndrome
D8943Secondary mast cell activation
D8949Other mast cell activation disorder
D8989Other specified disorders involving the immune mechanism, not elsewhere classified
D899Disorder involving the immune mechanism, unspecified
E320Persistent hyperplasia of thymus
E321Abscess of thymus
E328Other diseases of thymus
E329Disease of thymus, unspecified
I881Chronic lymphadenitis, except mesenteric
I888Other nonspecific lymphadenitis
I889Nonspecific lymphadenitis, unspecified
I898Other specified noninfective disorders of lymphatic vessels and lymph nodes
I899Noninfective disorder of lymphatic vessels and lymph nodes, unspecified
L040Acute lymphadenitis of face, head and neck
L041Acute lymphadenitis of trunk
L042Acute lymphadenitis of upper limb
L043Acute lymphadenitis of lower limb
L048Acute lymphadenitis of other sites
L049Acute lymphadenitis, unspecified
Q8901Asplenia (congenital)
Q8909Congenital malformations of spleen
R161Splenomegaly, not elsewhere classified
R590Localized enlarged lymph nodes
R591Generalized enlarged lymph nodes
R599Enlarged lymph nodes, unspecified
R75Inconclusive laboratory evidence of human immunodeficiency virus [HIV]
R760Raised antibody titer
R768Other specified abnormal immunological findings in serum
R769Abnormal immunological finding in serum, unspecified
S3600XAUnspecified injury of spleen, initial encounter
S36020AMinor contusion of spleen, initial encounter
S36021AMajor contusion of spleen, initial encounter
S36029AUnspecified contusion of spleen, initial encounter
S36030ASuperficial (capsular) laceration of spleen, initial encounter
S36031AModerate laceration of spleen, initial encounter
S36032AMajor laceration of spleen, initial encounter
S36039AUnspecified laceration of spleen, initial encounter
S3609XAOther injury of spleen, initial encounter
Z9481Bone marrow transplant status
Z9484Stem cells transplant status



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04 Oct 2018 16:21:08
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