Instructions: Using an ICD-10-CM code book, assign the proper diagnosis code to the following diagnostic statements...

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Instructions: Using an ICD-10-CM code book, assign the proper diagnosis code to the following diagnostic statements...

Instructions: Using an ICD-10-CM code book, assign the proper diagnosis code to the following diagnostic statements

sarcoidosis of the skin

hypergammaglobulinemia

DiGeorge's syndrome

biotin-dependent carboxylase deficiency

selective deficiency of IgA

cryoglobulinemia

sarcoid myositis

LFA-1 defect

Common variable immunodeficiency with predominant immunoregulatory T cell disorder

postprocedural complication of the spleen

microangiopathic hemolytic anemia

IgE syndrome

Wiskott-Aldrich syndrome

Nezelof's syndrome

iridocyclitis in sarcoidosis

polycythemia acquired

cyst of the spleen

intraoperative hemorrhage of the spleen, complicating a procedure

myelofibrosis

plasmacytosis

prothrombin gene mutation

congenital thrombocytopenia

protein C deficiency

fibrinolytic purpura

congenital Heinz body anemia

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Answer 1

Answer #1

ANSWER.

ICD-10-CM coding.

* Sarcoidosis of skin - D86.3

* Hypergammaglobulinemia - D89.2

* Digeorge's syndrome - D82.1

* Biotin dependent carboxylase deficiency - D81.819.

* Selective deficiency of Ig A - D80.2

* Cryoglobulinemia - D89.1

* Sarcoid myositis - D86.87.

* LFA-1 Defect - D84.0.

* Common variable immunodeficiency with predominant immuno

regulatory T cell disorder - D83.1

* Postprocedural complication of the spleen - D78.89.

* Microangiopathic hemolytic anemia - D59.4.

* IgE syndrome - D82.4.

* Wiskcott-Aldrich syndrome - D82.0

* Nezelof's syndrome - D81.4

* Iridocyclitis in sarcoidosis - D86.83

* Polycythemia acquired - D75.1

* Cyst of spleen - D73.4

* Intraoperative hemorrhage of spllen,complicating a procedure - D78.01

* Myelofibrosis - D75.81

* Plasmacytosis - D72.822

* Prothrombin gene mutation - D68.52

* Congenital thrombocytopenia - D69.42

* Protein c deficiency - D68.59

* Fibrinolytic purpura - D65

* Congenital heinz body anemia - D56.4

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Answer 2

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