Type 1 Excludes Crosswalk

The following 3,432 ICD-10-CM codes contain 'Type 1 Excludes' annotation references within one-to-many other ICD-10-CM codes.

Displaying codes 1,101-1,200 of 3,432:

  • D65: D69
    2020 ICD-10-CM Diagnosis Code D69

    Purpura and other hemorrhagic conditions

      2016 2017 2018 2019 2020 Non-Billable/Non-Specific Code
    Type 1 Excludes
    • benign hypergammaglobulinemic purpura (D89.0)
    • cryoglobulinemic purpura (D89.1)
    • essential (hemorrhagic) thrombocythemia (D47.3)
    • hemorrhagic thrombocythemia (D47.3)
    • purpura fulminans (D65)
    • thrombotic thrombocytopenic purpura (M31.1)
    • Waldenström hypergammaglobulinemic purpura (D89.0)
  • D66: D68.0
    , D68.0
    2020 ICD-10-CM Diagnosis Code D68.0

    Von Willebrand's disease

      2016 2017 2018 2019 2020 Billable/Specific Code
    Applicable To
    • Angiohemophilia
    • Factor VIII deficiency with vascular defect
    • Vascular hemophilia
    Type 1 Excludes
    • capillary fragility (hereditary) (D69.8)
    • factor VIII deficiency NOS (D66)
    • factor VIII deficiency with functional defect (D66)
    2020 ICD-10-CM Diagnosis Code D68.0

    Von Willebrand's disease

      2016 2017 2018 2019 2020 Billable/Specific Code
    Applicable To
    • Angiohemophilia
    • Factor VIII deficiency with vascular defect
    • Vascular hemophilia
    Type 1 Excludes
    • capillary fragility (hereditary) (D69.8)
    • factor VIII deficiency NOS (D66)
    • factor VIII deficiency with functional defect (D66)
  • D68: R79.1
    2020 ICD-10-CM Diagnosis Code R79.1

    Abnormal coagulation profile

      2016 2017 2018 2019 2020 Billable/Specific Code
    Applicable To
    • Abnormal or prolonged bleeding time
    • Abnormal or prolonged coagulation time
    • Abnormal or prolonged partial thromboplastin time [PTT]
    • Abnormal or prolonged prothrombin time [PT]
    Type 1 Excludes
    • coagulation defects (D68.-)
    Type 2 Excludes
    • abnormality of fluid, electrolyte or acid-base balance (E86-E87)
  • D68.0: D66
    , D69.1
    , R04.81
    2020 ICD-10-CM Diagnosis Code R04.81

    Acute idiopathic pulmonary hemorrhage in infants

      2016 2017 2018 2019 2020 Billable/Specific Code Pediatric Dx (0-17 years)
    Applicable To
    • AIPHI
    • Acute idiopathic hemorrhage in infants over 28 days old
    Type 1 Excludes
    • perinatal pulmonary hemorrhage (P26.-)
    • von Willebrand's disease (D68.0)
    2020 ICD-10-CM Diagnosis Code D69.1

    Qualitative platelet defects

      2016 2017 2018 2019 2020 Billable/Specific Code
    Applicable To
    • Bernard-Soulier [giant platelet] syndrome
    • Glanzmann's disease
    • Grey platelet syndrome
    • Thromboasthenia (hemorrhagic) (hereditary)
    • Thrombocytopathy
    Type 1 Excludes
    • von Willebrand's disease (D68.0)
    2020 ICD-10-CM Diagnosis Code D66

    Hereditary factor VIII deficiency

      2016 2017 2018 2019 2020 Billable/Specific Code
    Applicable To
    • Classical hemophilia
    • Deficiency factor VIII (with functional defect)
    • Hemophilia NOS
    • Hemophilia A
    Type 1 Excludes
    • factor VIII deficiency with vascular defect (D68.0)
  • D68.312: D68.5
    , D68.61
    , D68.62
    2020 ICD-10-CM Diagnosis Code D68.61

    Antiphospholipid syndrome

      2016 2017 2018 2019 2020 Billable/Specific Code
    Applicable To
    • Anticardiolipin syndrome
    • Antiphospholipid antibody syndrome
    Type 1 Excludes
    • anti-phospholipid antibody, finding without diagnosis (R76.0)
    • anti-phospholipid antibody with hemorrhagic disorder (D68.312)
    • lupus anticoagulant syndrome (D68.62)
    2020 ICD-10-CM Diagnosis Code D68.62

    Lupus anticoagulant syndrome

      2016 2017 2018 2019 2020 Billable/Specific Code
    Applicable To
    • Lupus anticoagulant
    • Presence of systemic lupus erythematosus [SLE] inhibitor
    Type 1 Excludes
    • anticardiolipin syndrome (D68.61)
    • antiphospholipid syndrome (D68.61)
    • lupus anticoagulant (LAC) finding without diagnosis (R76.0)
    • lupus anticoagulant (LAC) with hemorrhagic disorder (D68.312)
    2020 ICD-10-CM Diagnosis Code D68.5

    Primary thrombophilia

      2016 2017 2018 2019 2020 Non-Billable/Non-Specific Code
    Applicable To
    • Primary hypercoagulable states
    Type 1 Excludes
    • antiphospholipid syndrome (D68.61)
    • lupus anticoagulant (D68.62)
    • secondary activated protein C resistance (D68.69)
    • secondary antiphospholipid antibody syndrome (D68.69)
    • secondary lupus anticoagulant with hypercoagulable state (D68.69)
    • secondary systemic lupus erythematosus [SLE] inhibitor with hypercoagulable state (D68.69)
    • systemic lupus erythematosus [SLE] inhibitor finding without diagnosis (R76.0)
    • systemic lupus erythematosus [SLE] inhibitor with hemorrhagic disorder (D68.312)
    • thrombotic thrombocytopenic purpura (M31.1)
  • D68.4: E56.1
    2020 ICD-10-CM Diagnosis Code E56.1

    Deficiency of vitamin K

      2016 2017 2018 2019 2020 Billable/Specific Code
    Type 1 Excludes
    • deficiency of coagulation factor due to vitamin K deficiency (D68.4)
    • vitamin K deficiency of newborn (P53)
  • D68.61: D68.312
    , D68.312
    , D68.5
    , D68.62
    , D68.62
    2020 ICD-10-CM Diagnosis Code D68.5

    Primary thrombophilia

      2016 2017 2018 2019 2020 Non-Billable/Non-Specific Code
    Applicable To
    • Primary hypercoagulable states
    Type 1 Excludes
    • antiphospholipid syndrome (D68.61)
    • lupus anticoagulant (D68.62)
    • secondary activated protein C resistance (D68.69)
    • secondary antiphospholipid antibody syndrome (D68.69)
    • secondary lupus anticoagulant with hypercoagulable state (D68.69)
    • secondary systemic lupus erythematosus [SLE] inhibitor with hypercoagulable state (D68.69)
    • systemic lupus erythematosus [SLE] inhibitor finding without diagnosis (R76.0)
    • systemic lupus erythematosus [SLE] inhibitor with hemorrhagic disorder (D68.312)
    • thrombotic thrombocytopenic purpura (M31.1)
    2020 ICD-10-CM Diagnosis Code D68.62

    Lupus anticoagulant syndrome

      2016 2017 2018 2019 2020 Billable/Specific Code
    Applicable To
    • Lupus anticoagulant
    • Presence of systemic lupus erythematosus [SLE] inhibitor
    Type 1 Excludes
    • anticardiolipin syndrome (D68.61)
    • antiphospholipid syndrome (D68.61)
    • lupus anticoagulant (LAC) finding without diagnosis (R76.0)
    • lupus anticoagulant (LAC) with hemorrhagic disorder (D68.312)
    2020 ICD-10-CM Diagnosis Code D68.62

    Lupus anticoagulant syndrome

      2016 2017 2018 2019 2020 Billable/Specific Code
    Applicable To
    • Lupus anticoagulant
    • Presence of systemic lupus erythematosus [SLE] inhibitor
    Type 1 Excludes
    • anticardiolipin syndrome (D68.61)
    • antiphospholipid syndrome (D68.61)
    • lupus anticoagulant (LAC) finding without diagnosis (R76.0)
    • lupus anticoagulant (LAC) with hemorrhagic disorder (D68.312)
    2020 ICD-10-CM Diagnosis Code D68.312

    Antiphospholipid antibody with hemorrhagic disorder

      2016 2017 2018 2019 2020 Billable/Specific Code
    Applicable To
    • Lupus anticoagulant (LAC) with hemorrhagic disorder
    • Systemic lupus erythematosus [SLE] inhibitor with hemorrhagic disorder
    Type 1 Excludes
    • antiphospholipid antibody, finding without diagnosis (R76.0)
    • antiphospholipid antibody syndrome (D68.61)
    • antiphospholipid antibody with hypercoagulable state (D68.61)
    • lupus anticoagulant (LAC) finding without diagnosis (R76.0)
    • lupus anticoagulant (LAC) with hypercoagulable state (D68.62)
    • systemic lupus erythematosus [SLE] inhibitor finding without diagnosis (R76.0)
    • systemic lupus erythematosus [SLE] inhibitor with hypercoagulable state (D68.62)
    2020 ICD-10-CM Diagnosis Code D68.312

    Antiphospholipid antibody with hemorrhagic disorder

      2016 2017 2018 2019 2020 Billable/Specific Code
    Applicable To
    • Lupus anticoagulant (LAC) with hemorrhagic disorder
    • Systemic lupus erythematosus [SLE] inhibitor with hemorrhagic disorder
    Type 1 Excludes
    • antiphospholipid antibody, finding without diagnosis (R76.0)
    • antiphospholipid antibody syndrome (D68.61)
    • antiphospholipid antibody with hypercoagulable state (D68.61)
    • lupus anticoagulant (LAC) finding without diagnosis (R76.0)
    • lupus anticoagulant (LAC) with hypercoagulable state (D68.62)
    • systemic lupus erythematosus [SLE] inhibitor finding without diagnosis (R76.0)
    • systemic lupus erythematosus [SLE] inhibitor with hypercoagulable state (D68.62)
  • D68.62: D68.312
    , D68.312
    , D68.5
    , D68.61
    2020 ICD-10-CM Diagnosis Code D68.61

    Antiphospholipid syndrome

      2016 2017 2018 2019 2020 Billable/Specific Code
    Applicable To
    • Anticardiolipin syndrome
    • Antiphospholipid antibody syndrome
    Type 1 Excludes
    • anti-phospholipid antibody, finding without diagnosis (R76.0)
    • anti-phospholipid antibody with hemorrhagic disorder (D68.312)
    • lupus anticoagulant syndrome (D68.62)
    2020 ICD-10-CM Diagnosis Code D68.5

    Primary thrombophilia

      2016 2017 2018 2019 2020 Non-Billable/Non-Specific Code
    Applicable To
    • Primary hypercoagulable states
    Type 1 Excludes
    • antiphospholipid syndrome (D68.61)
    • lupus anticoagulant (D68.62)
    • secondary activated protein C resistance (D68.69)
    • secondary antiphospholipid antibody syndrome (D68.69)
    • secondary lupus anticoagulant with hypercoagulable state (D68.69)
    • secondary systemic lupus erythematosus [SLE] inhibitor with hypercoagulable state (D68.69)
    • systemic lupus erythematosus [SLE] inhibitor finding without diagnosis (R76.0)
    • systemic lupus erythematosus [SLE] inhibitor with hemorrhagic disorder (D68.312)
    • thrombotic thrombocytopenic purpura (M31.1)
    2020 ICD-10-CM Diagnosis Code D68.312

    Antiphospholipid antibody with hemorrhagic disorder

      2016 2017 2018 2019 2020 Billable/Specific Code
    Applicable To
    • Lupus anticoagulant (LAC) with hemorrhagic disorder
    • Systemic lupus erythematosus [SLE] inhibitor with hemorrhagic disorder
    Type 1 Excludes
    • antiphospholipid antibody, finding without diagnosis (R76.0)
    • antiphospholipid antibody syndrome (D68.61)
    • antiphospholipid antibody with hypercoagulable state (D68.61)
    • lupus anticoagulant (LAC) finding without diagnosis (R76.0)
    • lupus anticoagulant (LAC) with hypercoagulable state (D68.62)
    • systemic lupus erythematosus [SLE] inhibitor finding without diagnosis (R76.0)
    • systemic lupus erythematosus [SLE] inhibitor with hypercoagulable state (D68.62)
    2020 ICD-10-CM Diagnosis Code D68.312

    Antiphospholipid antibody with hemorrhagic disorder

      2016 2017 2018 2019 2020 Billable/Specific Code
    Applicable To
    • Lupus anticoagulant (LAC) with hemorrhagic disorder
    • Systemic lupus erythematosus [SLE] inhibitor with hemorrhagic disorder
    Type 1 Excludes
    • antiphospholipid antibody, finding without diagnosis (R76.0)
    • antiphospholipid antibody syndrome (D68.61)
    • antiphospholipid antibody with hypercoagulable state (D68.61)
    • lupus anticoagulant (LAC) finding without diagnosis (R76.0)
    • lupus anticoagulant (LAC) with hypercoagulable state (D68.62)
    • systemic lupus erythematosus [SLE] inhibitor finding without diagnosis (R76.0)
    • systemic lupus erythematosus [SLE] inhibitor with hypercoagulable state (D68.62)
  • D68.69: D68.5
    , D68.5
    , D68.5
    , D68.5
    2020 ICD-10-CM Diagnosis Code D68.5

    Primary thrombophilia

      2016 2017 2018 2019 2020 Non-Billable/Non-Specific Code
    Applicable To
    • Primary hypercoagulable states
    Type 1 Excludes
    • antiphospholipid syndrome (D68.61)
    • lupus anticoagulant (D68.62)
    • secondary activated protein C resistance (D68.69)
    • secondary antiphospholipid antibody syndrome (D68.69)
    • secondary lupus anticoagulant with hypercoagulable state (D68.69)
    • secondary systemic lupus erythematosus [SLE] inhibitor with hypercoagulable state (D68.69)
    • systemic lupus erythematosus [SLE] inhibitor finding without diagnosis (R76.0)
    • systemic lupus erythematosus [SLE] inhibitor with hemorrhagic disorder (D68.312)
    • thrombotic thrombocytopenic purpura (M31.1)
    2020 ICD-10-CM Diagnosis Code D68.5

    Primary thrombophilia

      2016 2017 2018 2019 2020 Non-Billable/Non-Specific Code
    Applicable To
    • Primary hypercoagulable states
    Type 1 Excludes
    • antiphospholipid syndrome (D68.61)
    • lupus anticoagulant (D68.62)
    • secondary activated protein C resistance (D68.69)
    • secondary antiphospholipid antibody syndrome (D68.69)
    • secondary lupus anticoagulant with hypercoagulable state (D68.69)
    • secondary systemic lupus erythematosus [SLE] inhibitor with hypercoagulable state (D68.69)
    • systemic lupus erythematosus [SLE] inhibitor finding without diagnosis (R76.0)
    • systemic lupus erythematosus [SLE] inhibitor with hemorrhagic disorder (D68.312)
    • thrombotic thrombocytopenic purpura (M31.1)
    2020 ICD-10-CM Diagnosis Code D68.5

    Primary thrombophilia

      2016 2017 2018 2019 2020 Non-Billable/Non-Specific Code
    Applicable To
    • Primary hypercoagulable states
    Type 1 Excludes
    • antiphospholipid syndrome (D68.61)
    • lupus anticoagulant (D68.62)
    • secondary activated protein C resistance (D68.69)
    • secondary antiphospholipid antibody syndrome (D68.69)
    • secondary lupus anticoagulant with hypercoagulable state (D68.69)
    • secondary systemic lupus erythematosus [SLE] inhibitor with hypercoagulable state (D68.69)
    • systemic lupus erythematosus [SLE] inhibitor finding without diagnosis (R76.0)
    • systemic lupus erythematosus [SLE] inhibitor with hemorrhagic disorder (D68.312)
    • thrombotic thrombocytopenic purpura (M31.1)
    2020 ICD-10-CM Diagnosis Code D68.5

    Primary thrombophilia

      2016 2017 2018 2019 2020 Non-Billable/Non-Specific Code
    Applicable To
    • Primary hypercoagulable states
    Type 1 Excludes
    • antiphospholipid syndrome (D68.61)
    • lupus anticoagulant (D68.62)
    • secondary activated protein C resistance (D68.69)
    • secondary antiphospholipid antibody syndrome (D68.69)
    • secondary lupus anticoagulant with hypercoagulable state (D68.69)
    • secondary systemic lupus erythematosus [SLE] inhibitor with hypercoagulable state (D68.69)
    • systemic lupus erythematosus [SLE] inhibitor finding without diagnosis (R76.0)
    • systemic lupus erythematosus [SLE] inhibitor with hemorrhagic disorder (D68.312)
    • thrombotic thrombocytopenic purpura (M31.1)
  • D69: R23.3
    2020 ICD-10-CM Diagnosis Code R23.3

    Spontaneous ecchymoses

      2016 2017 2018 2019 2020 Billable/Specific Code
    Applicable To
    • Petechiae
    Type 1 Excludes
  • D69.0: L95
    2020 ICD-10-CM Diagnosis Code L95

    Vasculitis limited to skin, not elsewhere classified

      2016 2017 2018 2019 2020 Non-Billable/Non-Specific Code
    Type 1 Excludes
    • angioma serpiginosum (L81.7)
    • Henoch(-Schönlein) purpura (D69.0)
    • hypersensitivity angiitis (M31.0)
    • lupus panniculitis (L93.2)
    • panniculitis NOS (M79.3)
    • panniculitis of neck and back (M54.0-)
    • polyarteritis nodosa (M30.0)
    • relapsing panniculitis (M35.6)
    • rheumatoid vasculitis (M05.2)
    • serum sickness (T80.6-)
    • urticaria (L50.-)
    • Wegener's granulomatosis (M31.3-)
  • D69.3: D69.0
    2020 ICD-10-CM Diagnosis Code D69.0

    Allergic purpura

      2016 2017 2018 2019 2020 Billable/Specific Code
    Applicable To
    • Allergic vasculitis
    • Nonthrombocytopenic hemorrhagic purpura
    • Nonthrombocytopenic idiopathic purpura
    • Purpura anaphylactoid
    • Purpura Henoch(-Schönlein)
    • Purpura rheumatica
    • Vascular purpura
    Type 1 Excludes
    • thrombocytopenic hemorrhagic purpura (D69.3)
  • D69.41: D59.1
    2020 ICD-10-CM Diagnosis Code D59.1

    Other autoimmune hemolytic anemias

      2016 2017 2018 2019 2020 Billable/Specific Code
    Applicable To
    • Autoimmune hemolytic disease (cold type) (warm type)
    • Chronic cold hemagglutinin disease
    • Cold agglutinin disease
    • Cold agglutinin hemoglobinuria
    • Cold type (secondary) (symptomatic) hemolytic anemia
    • Warm type (secondary) (symptomatic) hemolytic anemia
    Type 1 Excludes
    • Evans syndrome (D69.41)
    • hemolytic disease of newborn (P55.-)
    • paroxysmal cold hemoglobinuria (D59.6)
  • D69.8: D68.0
    2020 ICD-10-CM Diagnosis Code D68.0

    Von Willebrand's disease

      2016 2017 2018 2019 2020 Billable/Specific Code
    Applicable To
    • Angiohemophilia
    • Factor VIII deficiency with vascular defect
    • Vascular hemophilia
    Type 1 Excludes
    • capillary fragility (hereditary) (D69.8)
    • factor VIII deficiency NOS (D66)
    • factor VIII deficiency with functional defect (D66)
  • D70: D61
    , D72
    , D72.81
    2020 ICD-10-CM Diagnosis Code D72

    Other disorders of white blood cells

      2016 2017 2018 2019 2020 Non-Billable/Non-Specific Code
    Type 1 Excludes
    2020 ICD-10-CM Diagnosis Code D72.81

    Decreased white blood cell count

      2016 2017 2018 2019 2020 Non-Billable/Non-Specific Code
    Type 1 Excludes
    2020 ICD-10-CM Diagnosis Code D61

    Other aplastic anemias and other bone marrow failure syndromes

      2016 2017 2018 2019 2020 Non-Billable/Non-Specific Code
    Type 1 Excludes
  • D70.0: P61.5
    2020 ICD-10-CM Diagnosis Code P61.5

    Transient neonatal neutropenia

      2016 2017 2018 2019 2020 Billable/Specific Code Code on Newborn Record
    Type 1 Excludes
    • congenital neutropenia (nontransient) (D70.0)
  • D70.9: D72.819
    2020 ICD-10-CM Diagnosis Code D72.819

    Decreased white blood cell count, unspecified

      2016 2017 2018 2019 2020 Billable/Specific Code
    Applicable To
    • Decreased leukocytes, unspecified
    • Leukocytopenia, unspecified
    • Leukopenia
    Type 1 Excludes
    • malignant leukopenia (D70.9)
  • D72.1: D72.82
    2020 ICD-10-CM Diagnosis Code D72.82

    Elevated white blood cell count

      2016 2017 2018 2019 2020 Non-Billable/Non-Specific Code
    Type 1 Excludes
  • D72.824: D72
    2020 ICD-10-CM Diagnosis Code D72

    Other disorders of white blood cells

      2016 2017 2018 2019 2020 Non-Billable/Non-Specific Code
    Type 1 Excludes
  • D73.81: D70
    , D73.1
    , D73.1
    2020 ICD-10-CM Diagnosis Code D73.1

    Hypersplenism

      2016 2017 2018 2019 2020 Billable/Specific Code
    Type 1 Excludes
    • neutropenic splenomegaly (D73.81)
    • primary splenic neutropenia (D73.81)
    • splenitis, splenomegaly in late syphilis (A52.79)
    • splenitis, splenomegaly in tuberculosis (A18.85)
    • splenomegaly NOS (R16.1)
    • splenomegaly congenital (Q89.0)
    2020 ICD-10-CM Diagnosis Code D73.1

    Hypersplenism

      2016 2017 2018 2019 2020 Billable/Specific Code
    Type 1 Excludes
    • neutropenic splenomegaly (D73.81)
    • primary splenic neutropenia (D73.81)
    • splenitis, splenomegaly in late syphilis (A52.79)
    • splenitis, splenomegaly in tuberculosis (A18.85)
    • splenomegaly NOS (R16.1)
    • splenomegaly congenital (Q89.0)
    2020 ICD-10-CM Diagnosis Code D70

    Neutropenia

      2016 2017 2018 2019 2020 Non-Billable/Non-Specific Code
    Includes
    • agranulocytosis
    • decreased absolute neurophile count (ANC)
    Type 1 Excludes
    • neutropenic splenomegaly (D73.81)
    • transient neonatal neutropenia (P61.5)
    Use Additional
  • D74: D58.2
    2020 ICD-10-CM Diagnosis Code D58.2

    Other hemoglobinopathies

      2016 2017 2018 2019 2020 Billable/Specific Code
    Applicable To
    • Abnormal hemoglobin NOS
    • Congenital Heinz body anemia
    • Hb-C disease
    • Hb-D disease
    • Hb-E disease
    • Hemoglobinopathy NOS
    • Unstable hemoglobin hemolytic disease
    Type 1 Excludes
    • familial polycythemia (D75.0)
    • Hb-M disease (D74.0)
    • hemoglobin E-beta thalassemia (D56.5)
    • hereditary persistence of fetal hemoglobin [HPFH] (D56.4)
    • high-altitude polycythemia (D75.1)
    • methemoglobinemia (D74.-)
    • other hemoglobinopathies with thalassemia (D56.8)
  • D74.0: D58.2
    2020 ICD-10-CM Diagnosis Code D58.2

    Other hemoglobinopathies

      2016 2017 2018 2019 2020 Billable/Specific Code
    Applicable To
    • Abnormal hemoglobin NOS
    • Congenital Heinz body anemia
    • Hb-C disease
    • Hb-D disease
    • Hb-E disease
    • Hemoglobinopathy NOS
    • Unstable hemoglobin hemolytic disease
    Type 1 Excludes
    • familial polycythemia (D75.0)
    • Hb-M disease (D74.0)
    • hemoglobin E-beta thalassemia (D56.5)
    • hereditary persistence of fetal hemoglobin [HPFH] (D56.4)
    • high-altitude polycythemia (D75.1)
    • methemoglobinemia (D74.-)
    • other hemoglobinopathies with thalassemia (D56.8)
  • D75.0: D45
    , D58.2
    , R71
    2020 ICD-10-CM Diagnosis Code D58.2

    Other hemoglobinopathies

      2016 2017 2018 2019 2020 Billable/Specific Code
    Applicable To
    • Abnormal hemoglobin NOS
    • Congenital Heinz body anemia
    • Hb-C disease
    • Hb-D disease
    • Hb-E disease
    • Hemoglobinopathy NOS
    • Unstable hemoglobin hemolytic disease
    Type 1 Excludes
    • familial polycythemia (D75.0)
    • Hb-M disease (D74.0)
    • hemoglobin E-beta thalassemia (D56.5)
    • hereditary persistence of fetal hemoglobin [HPFH] (D56.4)
    • high-altitude polycythemia (D75.1)
    • methemoglobinemia (D74.-)
    • other hemoglobinopathies with thalassemia (D56.8)
    2020 ICD-10-CM Diagnosis Code D45

    Polycythemia vera

      2016 2017 2018 2019 2020 Billable/Specific Code
    Type 1 Excludes
    • familial polycythemia (D75.0)
    • secondary polycythemia (D75.1)
    2020 ICD-10-CM Diagnosis Code R71

    Abnormality of red blood cells

      2016 2017 2018 2019 2020 Non-Billable/Non-Specific Code
    Type 1 Excludes
    • anemias (D50-D64)
    • anemia of premature infant (P61.2)
    • benign (familial) polycythemia (D75.0)
    • congenital anemias (P61.2-P61.4)
    • newborn anemia due to isoimmunization (P55.-)
    • polycythemia neonatorum (P61.1)
    • polycythemia NOS (D75.1)
    • polycythemia vera (D45)
    • secondary polycythemia (D75.1)
  • D75.1: D45
    , D58.2
    , R71
    , R71
    2020 ICD-10-CM Diagnosis Code R71

    Abnormality of red blood cells

      2016 2017 2018 2019 2020 Non-Billable/Non-Specific Code
    Type 1 Excludes
    • anemias (D50-D64)
    • anemia of premature infant (P61.2)
    • benign (familial) polycythemia (D75.0)
    • congenital anemias (P61.2-P61.4)
    • newborn anemia due to isoimmunization (P55.-)
    • polycythemia neonatorum (P61.1)
    • polycythemia NOS (D75.1)
    • polycythemia vera (D45)
    • secondary polycythemia (D75.1)
    2020 ICD-10-CM Diagnosis Code R71

    Abnormality of red blood cells

      2016 2017 2018 2019 2020 Non-Billable/Non-Specific Code
    Type 1 Excludes
    • anemias (D50-D64)
    • anemia of premature infant (P61.2)
    • benign (familial) polycythemia (D75.0)
    • congenital anemias (P61.2-P61.4)
    • newborn anemia due to isoimmunization (P55.-)
    • polycythemia neonatorum (P61.1)
    • polycythemia NOS (D75.1)
    • polycythemia vera (D45)
    • secondary polycythemia (D75.1)
    2020 ICD-10-CM Diagnosis Code D45

    Polycythemia vera

      2016 2017 2018 2019 2020 Billable/Specific Code
    Type 1 Excludes
    • familial polycythemia (D75.0)
    • secondary polycythemia (D75.1)
    2020 ICD-10-CM Diagnosis Code D58.2

    Other hemoglobinopathies

      2016 2017 2018 2019 2020 Billable/Specific Code
    Applicable To
    • Abnormal hemoglobin NOS
    • Congenital Heinz body anemia
    • Hb-C disease
    • Hb-D disease
    • Hb-E disease
    • Hemoglobinopathy NOS
    • Unstable hemoglobin hemolytic disease
    Type 1 Excludes
    • familial polycythemia (D75.0)
    • Hb-M disease (D74.0)
    • hemoglobin E-beta thalassemia (D56.5)
    • hereditary persistence of fetal hemoglobin [HPFH] (D56.4)
    • high-altitude polycythemia (D75.1)
    • methemoglobinemia (D74.-)
    • other hemoglobinopathies with thalassemia (D56.8)
  • D75.81: C94.4
    , C94.4
    , D47.1
    , D47.1
    , D61.82
    , D61.82
    , M85.8
    2020 ICD-10-CM Diagnosis Code D61.82

    Myelophthisis

      2016 2017 2018 2019 2020 Billable/Specific Code
    Applicable To
    • Leukoerythroblastic anemia
    • Myelophthisic anemia
    • Panmyelophthisis
    Code Also
    • the underlying disorder, such as:
    • malignant neoplasm of breast (C50.-)
    • tuberculosis (A15.-)
    Type 1 Excludes
    • idiopathic myelofibrosis (D47.1)
    • myelofibrosis NOS (D75.81)
    • myelofibrosis with myeloid metaplasia (D47.4)
    • primary myelofibrosis (D47.1)
    • secondary myelofibrosis (D75.81)
    2020 ICD-10-CM Diagnosis Code D61.82

    Myelophthisis

      2016 2017 2018 2019 2020 Billable/Specific Code
    Applicable To
    • Leukoerythroblastic anemia
    • Myelophthisic anemia
    • Panmyelophthisis
    Code Also
    • the underlying disorder, such as:
    • malignant neoplasm of breast (C50.-)
    • tuberculosis (A15.-)
    Type 1 Excludes
    • idiopathic myelofibrosis (D47.1)
    • myelofibrosis NOS (D75.81)
    • myelofibrosis with myeloid metaplasia (D47.4)
    • primary myelofibrosis (D47.1)
    • secondary myelofibrosis (D75.81)
    2020 ICD-10-CM Diagnosis Code D47.1

    Chronic myeloproliferative disease

      2016 2017 2018 2019 2020 Billable/Specific Code
    Applicable To
    • Chronic neutrophilic leukemia
    • Myeloproliferative disease, unspecified
    Type 1 Excludes
    • atypical chronic myeloid leukemia BCR/ABL-negative (C92.2-)
    • chronic myeloid leukemia BCR/ABL-positive (C92.1-)
    • myelofibrosis NOS (D75.81)
    • myelophthisic anemia (D61.82)
    • myelophthisis (D61.82)
    • secondary myelofibrosis NOS (D75.81)
    2020 ICD-10-CM Diagnosis Code D47.1

    Chronic myeloproliferative disease

      2016 2017 2018 2019 2020 Billable/Specific Code
    Applicable To
    • Chronic neutrophilic leukemia
    • Myeloproliferative disease, unspecified
    Type 1 Excludes
    • atypical chronic myeloid leukemia BCR/ABL-negative (C92.2-)
    • chronic myeloid leukemia BCR/ABL-positive (C92.1-)
    • myelofibrosis NOS (D75.81)
    • myelophthisic anemia (D61.82)
    • myelophthisis (D61.82)
    • secondary myelofibrosis NOS (D75.81)
    2020 ICD-10-CM Diagnosis Code M85.8

    Other specified disorders of bone density and structure

      2016 2017 2018 2019 2020 Non-Billable/Non-Specific Code
    Applicable To
    • Hyperostosis of bones, except skull
    • Osteosclerosis, acquired
    Type 1 Excludes
    • diffuse idiopathic skeletal hyperostosis [DISH] (M48.1)
    • osteosclerosis congenita (Q77.4)
    • osteosclerosis fragilitas (generalista) (Q78.2)
    • osteosclerosis myelofibrosis (D75.81)
    2020 ICD-10-CM Diagnosis Code C94.4

    Acute panmyelosis with myelofibrosis

      2016 2017 2018 2019 2020 Non-Billable/Non-Specific Code
    Applicable To
    • Acute myelofibrosis
    Type 1 Excludes
    • myelofibrosis NOS (D75.81)
    • secondary myelofibrosis NOS (D75.81)
    2020 ICD-10-CM Diagnosis Code C94.4

    Acute panmyelosis with myelofibrosis

      2016 2017 2018 2019 2020 Non-Billable/Non-Specific Code
    Applicable To
    • Acute myelofibrosis
    Type 1 Excludes
    • myelofibrosis NOS (D75.81)
    • secondary myelofibrosis NOS (D75.81)
  • D75.82: D68.6
    , D69.5
    2020 ICD-10-CM Diagnosis Code D68.6

    Other thrombophilia

      2016 2017 2018 2019 2020 Non-Billable/Non-Specific Code
    Applicable To
    • Other hypercoagulable states
    Type 1 Excludes
    • diffuse or disseminated intravascular coagulation [DIC] (D65)
    • heparin induced thrombocytopenia (HIT) (D75.82)
    • hyperhomocysteinemia (E72.11)
    2020 ICD-10-CM Diagnosis Code D69.5

    Secondary thrombocytopenia

      2016 2017 2018 2019 2020 Non-Billable/Non-Specific Code
    Type 1 Excludes
    • heparin induced thrombocytopenia (HIT) (D75.82)
    • transient thrombocytopenia of newborn (P61.0)
  • D75.A: D55.0
    2020 ICD-10-CM Diagnosis Code D55.0

    Anemia due to glucose-6-phosphate dehydrogenase [G6PD] deficiency

      2016 2017 2018 2019 2020 Billable/Specific Code
    Applicable To
    • Favism
    • G6PD deficiency anemia
    Type 1 Excludes
    • glucose-6-phosphate dehydrogenase (G6PD) deficiency without anemia (D75.A)
  • D78.1: D78.0
    2020 ICD-10-CM Diagnosis Code D78.0

    Intraoperative hemorrhage and hematoma of the spleen complicating a procedure

      2016 2017 2018 2019 2020 Non-Billable/Non-Specific Code
    Type 1 Excludes
    • intraoperative hemorrhage and hematoma of the spleen due to accidental puncture or laceration during a procedure (D78.1-)
  • D80.0: D81
    2020 ICD-10-CM Diagnosis Code D81

    Combined immunodeficiencies

      2016 2017 2018 2019 2020 Non-Billable/Non-Specific Code
    Type 1 Excludes
    • autosomal recessive agammaglobulinemia (Swiss type) (D80.0)
  • D80.7: P61
    2020 ICD-10-CM Diagnosis Code P61

    Other perinatal hematological disorders

      2016 2017 2018 2019 2020 Non-Billable/Non-Specific Code
    Type 1 Excludes
    • transient hypogammaglobulinemia of infancy (D80.7)
  • D81: E79
    2020 ICD-10-CM Diagnosis Code E79

    Disorders of purine and pyrimidine metabolism

      2016 2017 2018 2019 2020 Non-Billable/Non-Specific Code
    Type 1 Excludes
  • D82.0: D69.4
    2020 ICD-10-CM Diagnosis Code D69.4

    Other primary thrombocytopenia

      2016 2017 2018 2019 2020 Non-Billable/Non-Specific Code
    Type 1 Excludes
    • transient neonatal thrombocytopenia (P61.0)
    • Wiskott-Aldrich syndrome (D82.0)
  • D82.1: E20
    , E32
    , E32.8
    , Q38.7
    2020 ICD-10-CM Diagnosis Code E32

    Diseases of thymus

      2016 2017 2018 2019 2020 Non-Billable/Non-Specific Code
    Type 1 Excludes
    • aplasia or hypoplasia of thymus with immunodeficiency (D82.1)
    • myasthenia gravis (G70.0)
    2020 ICD-10-CM Diagnosis Code E32.8

    Other diseases of thymus

      2016 2017 2018 2019 2020 Billable/Specific Code
    Type 1 Excludes
    • aplasia or hypoplasia with immunodeficiency (D82.1)
    • thymoma (D15.0)
    2020 ICD-10-CM Diagnosis Code E20

    Hypoparathyroidism

      2016 2017 2018 2019 2020 Non-Billable/Non-Specific Code
    Type 1 Excludes
    • Di George's syndrome (D82.1)
    • postprocedural hypoparathyroidism (E89.2)
    • tetany NOS (R29.0)
    • transitory neonatal hypoparathyroidism (P71.4)
    2020 ICD-10-CM Diagnosis Code Q38.7

    Congenital pharyngeal pouch

      2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
    Applicable To
    • Congenital diverticulum of pharynx
    Type 1 Excludes
    • pharyngeal pouch syndrome (D82.1)
  • D82.2: E34.3
    2020 ICD-10-CM Diagnosis Code E34.3

    Short stature due to endocrine disorder

      2016 2017 2018 2019 2020 Billable/Specific Code
    Applicable To
    • Constitutional short stature
    • Laron-type short stature
    Type 1 Excludes
    • achondroplastic short stature (Q77.4)
    • hypochondroplastic short stature (Q77.4)
    • nutritional short stature (E45)
    • pituitary short stature (E23.0)
    • progeria (E34.8)
    • renal short stature (N25.0)
    • Russell-Silver syndrome (Q87.19)
    • short-limbed stature with immunodeficiency (D82.2)
    • short stature in specific dysmorphic syndromes - code to syndrome - see Alphabetical Index
    • short stature NOS (R62.52)
  • D84.1: L50
    2020 ICD-10-CM Diagnosis Code L50

    Urticaria

      2016 2017 2018 2019 2020 Non-Billable/Non-Specific Code
    Type 1 Excludes
    • allergic contact dermatitis (L23.-)
    • angioneurotic edema (T78.3)
    • giant urticaria (T78.3)
    • hereditary angio-edema (D84.1)
    • Quincke's edema (T78.3)
    • serum urticaria (T80.6-)
    • solar urticaria (L56.3)
    • urticaria neonatorum (P83.8)
    • urticaria papulosa (L28.2)
    • urticaria pigmentosa (D47.01)
  • D86.82: G53
    2020 ICD-10-CM Diagnosis Code G53

    Cranial nerve disorders in diseases classified elsewhere

      2016 2017 2018 2019 2020 Billable/Specific Code Manifestation Code
    Code First
    • underlying disease, such as:
    • neoplasm (C00-D49)
    Type 1 Excludes
    • multiple cranial nerve palsy in sarcoidosis (D86.82)
    • multiple cranial nerve palsy in syphilis (A52.15)
    • postherpetic geniculate ganglionitis (B02.21)
    • postherpetic trigeminal neuralgia (B02.22)
  • D86.83: H20.0
    2020 ICD-10-CM Diagnosis Code H20.0

    Acute and subacute iridocyclitis

      2016 2017 2018 2019 2020 Non-Billable/Non-Specific Code
    Applicable To
    • Acute anterior uveitis
    • Acute cyclitis
    • Acute iritis
    • Subacute anterior uveitis
    • Subacute cyclitis
    • Subacute iritis
    Type 1 Excludes
    • iridocyclitis, iritis, uveitis (due to) (in) diabetes mellitus (E08-E13 with .39)
    • iridocyclitis, iritis, uveitis (due to) (in) diphtheria (A36.89)
    • iridocyclitis, iritis, uveitis (due to) (in) gonococcal (A54.32)
    • iridocyclitis, iritis, uveitis (due to) (in) herpes (simplex) (B00.51)
    • iridocyclitis, iritis, uveitis (due to) (in) herpes zoster (B02.32)
    • iridocyclitis, iritis, uveitis (due to) (in) late congenital syphilis (A50.39)
    • iridocyclitis, iritis, uveitis (due to) (in) late syphilis (A52.71)
    • iridocyclitis, iritis, uveitis (due to) (in) sarcoidosis (D86.83)
    • iridocyclitis, iritis, uveitis (due to) (in) syphilis (A51.43)
    • iridocyclitis, iritis, uveitis (due to) (in) toxoplasmosis (B58.09)
    • iridocyclitis, iritis, uveitis (due to) (in) tuberculosis (A18.54)
  • D86.84: N16
    2020 ICD-10-CM Diagnosis Code N16

    Renal tubulo-interstitial disorders in diseases classified elsewhere

      2016 2017 2018 2019 2020 Billable/Specific Code Manifestation Code
    Applicable To
    • Pyelonephritis
    • Tubulo-interstitial nephritis
    Code First
    Type 1 Excludes
    • diphtheritic pyelonephritis and tubulo-interstitial nephritis (A36.84)
    • pyelonephritis and tubulo-interstitial nephritis in candidiasis (B37.49)
    • pyelonephritis and tubulo-interstitial nephritis in cystinosis (E72.04)
    • pyelonephritis and tubulo-interstitial nephritis in salmonella infection (A02.25)
    • pyelonephritis and tubulo-interstitial nephritis in sarcoidosis (D86.84)
    • pyelonephritis and tubulo-interstitial nephritis in sicca syndrome [Sjogren's] (M35.04)
    • pyelonephritis and tubulo-interstitial nephritis in systemic lupus erythematosus (M32.15)
    • pyelonephritis and tubulo-interstitial nephritis in toxoplasmosis (B58.83)
    • renal tubular degeneration in diabetes (E08-E13 with .29)
    • syphilitic pyelonephritis and tubulo-interstitial nephritis (A52.75)
  • D86.85: I41
    , I43
    2020 ICD-10-CM Diagnosis Code I43

    Cardiomyopathy in diseases classified elsewhere

      2016 2017 2018 2019 2020 Billable/Specific Code Manifestation Code
    Code First
    Type 1 Excludes
    2020 ICD-10-CM Diagnosis Code I41

    Myocarditis in diseases classified elsewhere

      2016 2017 2018 2019 2020 Billable/Specific Code Manifestation Code
    Code First
    Type 1 Excludes
  • D86.86: M01
    , M14
    2020 ICD-10-CM Diagnosis Code M01

    Direct infections of joint in infectious and parasitic diseases classified elsewhere

      2016 2017 2018 2019 2020 Non-Billable/Non-Specific Code
    Code First
    Type 1 Excludes
    2020 ICD-10-CM Diagnosis Code M14

    Arthropathies in other diseases classified elsewhere

      2016 2017 2018 2019 2020 Non-Billable/Non-Specific Code
    Type 1 Excludes
    • arthropathy in:
    • diabetes mellitus (E08-E13 with .61-)
    • hematological disorders (M36.2-M36.3)
    • hypersensitivity reactions (M36.4)
    • neoplastic disease (M36.1)
    • neurosyphillis (A52.16)
    • sarcoidosis (D86.86)
    • enteropathic arthropathies (M07.-)
    • juvenile psoriatic arthropathy (L40.54)
    • lipoid dermatoarthritis (E78.81)
  • D86.87: G73.7
    , M63
    2020 ICD-10-CM Diagnosis Code G73.7

    Myopathy in diseases classified elsewhere

      2016 2017 2018 2019 2020 Billable/Specific Code Manifestation Code
    Code First
    • underlying disease, such as:
    • hyperparathyroidism (E21.0, E21.3)
    • hypoparathyroidism (E20.-)
    • glycogen storage disease (E74.0)
    • lipid storage disorders (E75.-)
    Type 1 Excludes
    • myopathy in:
    • rheumatoid arthritis (M05.32)
    • sarcoidosis (D86.87)
    • scleroderma (M34.82)
    • sicca syndrome [Sjögren] (M35.03)
    • systemic lupus erythematosus (M32.19)
    2020 ICD-10-CM Diagnosis Code M63

    Disorders of muscle in diseases classified elsewhere

      2016 2017 2018 2019 2020 Non-Billable/Non-Specific Code
    Code First
    Type 1 Excludes
    • myopathy in cysticercosis (B69.81)
    • myopathy in endocrine diseases (G73.7)
    • myopathy in metabolic diseases (G73.7)
    • myopathy in sarcoidosis (D86.87)
    • myopathy in secondary syphilis (A51.49)
    • myopathy in syphilis (late) (A52.78)
    • myopathy in toxoplasmosis (B58.82)
    • myopathy in tuberculosis (A18.09)
  • D86.89: K11.2
    , K77
    2020 ICD-10-CM Diagnosis Code K11.2

    Sialoadenitis

      2016 2017 2018 2019 2020 Non-Billable/Non-Specific Code
    Applicable To
    • Parotitis
    Type 1 Excludes
    2020 ICD-10-CM Diagnosis Code K77

    Liver disorders in diseases classified elsewhere

      2016 2017 2018 2019 2020 Billable/Specific Code Manifestation Code
    Code First
    Type 1 Excludes
    • alcoholic hepatitis (K70.1-)
    • alcoholic liver disease (K70.-)
    • cytomegaloviral hepatitis (B25.1)
    • herpesviral [herpes simplex] hepatitis (B00.81)
    • infectious mononucleosis with liver disease (B27.0-B27.9 with .9)
    • mumps hepatitis (B26.81)
    • sarcoidosis with liver disease (D86.89)
    • secondary syphilis with liver disease (A51.45)
    • syphilis (late) with liver disease (A52.74)
    • toxoplasmosis (acquired) hepatitis (B58.1)
    • tuberculosis with liver disease (A18.83)
  • D89.0: D69
    , D69
    , E88.0
    2020 ICD-10-CM Diagnosis Code D69

    Purpura and other hemorrhagic conditions

      2016 2017 2018 2019 2020 Non-Billable/Non-Specific Code
    Type 1 Excludes
    • benign hypergammaglobulinemic purpura (D89.0)
    • cryoglobulinemic purpura (D89.1)
    • essential (hemorrhagic) thrombocythemia (D47.3)
    • hemorrhagic thrombocythemia (D47.3)
    • purpura fulminans (D65)
    • thrombotic thrombocytopenic purpura (M31.1)
    • Waldenström hypergammaglobulinemic purpura (D89.0)
    2020 ICD-10-CM Diagnosis Code D69

    Purpura and other hemorrhagic conditions

      2016 2017 2018 2019 2020 Non-Billable/Non-Specific Code
    Type 1 Excludes
    • benign hypergammaglobulinemic purpura (D89.0)
    • cryoglobulinemic purpura (D89.1)
    • essential (hemorrhagic) thrombocythemia (D47.3)
    • hemorrhagic thrombocythemia (D47.3)
    • purpura fulminans (D65)
    • thrombotic thrombocytopenic purpura (M31.1)
    • Waldenström hypergammaglobulinemic purpura (D89.0)
    2020 ICD-10-CM Diagnosis Code E88.0

    Disorders of plasma-protein metabolism, not elsewhere classified

      2016 2017 2018 2019 2020 Non-Billable/Non-Specific Code
    Type 1 Excludes
    • disorder of lipoprotein metabolism (E78.-)
    • monoclonal gammopathy (of undetermined significance) (D47.2)
    • polyclonal hypergammaglobulinemia (D89.0)
    • Waldenström macroglobulinemia (C88.0)
  • D89.1: D69
    2020 ICD-10-CM Diagnosis Code D69

    Purpura and other hemorrhagic conditions

      2016 2017 2018 2019 2020 Non-Billable/Non-Specific Code
    Type 1 Excludes
    • benign hypergammaglobulinemic purpura (D89.0)
    • cryoglobulinemic purpura (D89.1)
    • essential (hemorrhagic) thrombocythemia (D47.3)
    • hemorrhagic thrombocythemia (D47.3)
    • purpura fulminans (D65)
    • thrombotic thrombocytopenic purpura (M31.1)
    • Waldenström hypergammaglobulinemic purpura (D89.0)
  • E00: E01
    2020 ICD-10-CM Diagnosis Code E01

    Iodine-deficiency related thyroid disorders and allied conditions

      2016 2017 2018 2019 2020 Non-Billable/Non-Specific Code
    Type 1 Excludes
    • congenital iodine-deficiency syndrome (E00.-)
    • subclinical iodine-deficiency hypothyroidism (E02)
  • E02: E00
    , E01
    2020 ICD-10-CM Diagnosis Code E01

    Iodine-deficiency related thyroid disorders and allied conditions

      2016 2017 2018 2019 2020 Non-Billable/Non-Specific Code
    Type 1 Excludes
    • congenital iodine-deficiency syndrome (E00.-)
    • subclinical iodine-deficiency hypothyroidism (E02)
    2020 ICD-10-CM Diagnosis Code E00

    Congenital iodine-deficiency syndrome

      2016 2017 2018 2019 2020 Non-Billable/Non-Specific Code
    Type 1 Excludes
    • subclinical iodine-deficiency hypothyroidism (E02)
    Use Additional
    • code (F70-F79) to identify associated intellectual disabilities.
  • E03.0: E04
    , P72
    , Q89.2
    2020 ICD-10-CM Diagnosis Code E04

    Other nontoxic goiter

      2016 2017 2018 2019 2020 Non-Billable/Non-Specific Code
    Type 1 Excludes
    • congenital goiter (NOS) (diffuse) (parenchymatous) (E03.0)
    • iodine-deficiency related goiter (E00-E02)
    2020 ICD-10-CM Diagnosis Code P72

    Other transitory neonatal endocrine disorders

      2016 2017 2018 2019 2020 Non-Billable/Non-Specific Code
    Type 1 Excludes
    • congenital hypothyroidism with or without goiter (E03.0-E03.1)
    • dyshormogenetic goiter (E07.1)
    • Pendred's syndrome (E07.1)
    2020 ICD-10-CM Diagnosis Code Q89.2

    Congenital malformations of other endocrine glands

      2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
    Applicable To
    • Congenital malformation of parathyroid or thyroid gland
    • Persistent thyroglossal duct
    • Thyroglossal cyst
    Type 1 Excludes
    • congenital goiter (E03.0)
    • congenital hypothyroidism (E03.1)
  • E03.1: E03.4
    , P72
    , Q89.2
    2020 ICD-10-CM Diagnosis Code Q89.2

    Congenital malformations of other endocrine glands

      2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
    Applicable To
    • Congenital malformation of parathyroid or thyroid gland
    • Persistent thyroglossal duct
    • Thyroglossal cyst
    Type 1 Excludes
    • congenital goiter (E03.0)
    • congenital hypothyroidism (E03.1)
    2020 ICD-10-CM Diagnosis Code P72

    Other transitory neonatal endocrine disorders

      2016 2017 2018 2019 2020 Non-Billable/Non-Specific Code
    Type 1 Excludes
    • congenital hypothyroidism with or without goiter (E03.0-E03.1)
    • dyshormogenetic goiter (E07.1)
    • Pendred's syndrome (E07.1)
    2020 ICD-10-CM Diagnosis Code E03.4

    Atrophy of thyroid (acquired)

      2016 2017 2018 2019 2020 Billable/Specific Code
    Type 1 Excludes
    • congenital atrophy of thyroid (E03.1)
  • E03.9: L98.5
    2020 ICD-10-CM Diagnosis Code L98.5

    Mucinosis of the skin

      2016 2017 2018 2019 2020 Billable/Specific Code
    Applicable To
    • Focal mucinosis
    • Lichen myxedematosus
    • Reticular erythematous mucinosis
    Type 1 Excludes
  • E05.8: E22
    2020 ICD-10-CM Diagnosis Code E22

    Hyperfunction of pituitary gland

      2016 2017 2018 2019 2020 Non-Billable/Non-Specific Code
    Type 1 Excludes
    • Cushing's syndrome (E24.-)
    • Nelson's syndrome (E24.1)
    • overproduction of ACTH not associated with Cushing's disease (E27.0)
    • overproduction of pituitary ACTH (E24.0)
    • overproduction of thyroid-stimulating hormone (E05.8-)
  • E06.2: E05
    2020 ICD-10-CM Diagnosis Code E05

    Thyrotoxicosis [hyperthyroidism]

      2016 2017 2018 2019 2020 Non-Billable/Non-Specific Code
    Type 1 Excludes
    • chronic thyroiditis with transient thyrotoxicosis (E06.2)
    • neonatal thyrotoxicosis (P72.1)
  • E06.3: E06.1
    , E06.2
    2020 ICD-10-CM Diagnosis Code E06.2

    Chronic thyroiditis with transient thyrotoxicosis

      2016 2017 2018 2019 2020 Billable/Specific Code
    Type 1 Excludes
    • autoimmune thyroiditis (E06.3)
    2020 ICD-10-CM Diagnosis Code E06.1

    Subacute thyroiditis

      2016 2017 2018 2019 2020 Billable/Specific Code
    Applicable To
    • de Quervain thyroiditis
    • Giant-cell thyroiditis
    • Granulomatous thyroiditis
    • Nonsuppurative thyroiditis
    • Viral thyroiditis
    Type 1 Excludes
    • autoimmune thyroiditis (E06.3)
  • E07.1: P72
    , P72
    2020 ICD-10-CM Diagnosis Code P72

    Other transitory neonatal endocrine disorders

      2016 2017 2018 2019 2020 Non-Billable/Non-Specific Code
    Type 1 Excludes
    • congenital hypothyroidism with or without goiter (E03.0-E03.1)
    • dyshormogenetic goiter (E07.1)
    • Pendred's syndrome (E07.1)
    2020 ICD-10-CM Diagnosis Code P72

    Other transitory neonatal endocrine disorders

      2016 2017 2018 2019 2020 Non-Billable/Non-Specific Code
    Type 1 Excludes
    • congenital hypothyroidism with or without goiter (E03.0-E03.1)
    • dyshormogenetic goiter (E07.1)
    • Pendred's syndrome (E07.1)