2020 ICD-10-CM Diagnosis Code D58.1

Hereditary elliptocytosis

    2016 2017 2018 2019 2020 Billable/Specific Code
  • D58.1 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
  • The 2020 edition of ICD-10-CM D58.1 became effective on October 1, 2019.
  • This is the American ICD-10-CM version of D58.1 - other international versions of ICD-10 D58.1 may differ.
Applicable To
  • Elliptocytosis (congenital)
  • Ovalocytosis (congenital) (hereditary)
The following code(s) above D58.1 contain annotation back-references
Annotation Back-References
In this context, annotation back-references refer to codes that contain:
  • Applicable To annotations, or
  • Code Also annotations, or
  • Code First annotations, or
  • Excludes1 annotations, or
  • Excludes2 annotations, or
  • Includes annotations, or
  • Note annotations, or
  • Use Additional annotations
that may be applicable to D58.1:
  • D50-D89
    2020 ICD-10-CM Range D50-D89

    Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism

    Type 2 Excludes
    • autoimmune disease (systemic) NOS (M35.9)
    • certain conditions originating in the perinatal period (P00-P96)
    • complications of pregnancy, childbirth and the puerperium (O00-O9A)
    • congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
    • endocrine, nutritional and metabolic diseases (E00-E88)
    • human immunodeficiency virus [HIV] disease (B20)
    • injury, poisoning and certain other consequences of external causes (S00-T88)
    • neoplasms (C00-D49)
    • symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94)
    Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism
  • D58
    ICD-10-CM Diagnosis Code D58

    Other hereditary hemolytic anemias

      2016 2017 2018 2019 2020 Non-Billable/Non-Specific Code
    Type 1 Excludes
    • hemolytic anemia of the newborn (P55.-)
    Other hereditary hemolytic anemias
Approximate Synonyms
  • Elliptocytosis, hereditary
Clinical Information
  • A peripheral blood finding in which a large number of erythrocytes are shaped in a slightly oval-shaped form.
  • An intrinsic defect of erythrocytes inherited as an autosomal dominant trait. The erythrocytes assume an oval or elliptical shape.
  • Intrinsic defect of erythrocytes inherited as an autosomal dominant trait; erythrocytes assume an oval or elliptical shape.
ICD-10-CM D58.1 is grouped within Diagnostic Related Group(s) (MS-DRG v37.0):
  • 811 Red blood cell disorders with mcc
  • 812 Red blood cell disorders without mcc

Convert D58.1 to ICD-9-CM

Code History
  • 2016 (effective 10/1/2015): New code (first year of non-draft ICD-10-CM)
  • 2017 (effective 10/1/2016): No change
  • 2018 (effective 10/1/2017): No change
  • 2019 (effective 10/1/2018): No change
  • 2020 (effective 10/1/2019): No change
Code annotations containing back-references to D58.1:
  • Type 1 Excludes: D75.0
    ICD-10-CM Diagnosis Code D75.0

    Familial erythrocytosis

      2016 2017 2018 2019 2020 Billable/Specific Code
    Applicable To
    • Benign polycythemia
    • Familial polycythemia
    Type 1 Excludes
    • hereditary ovalocytosis (D58.1)

Diagnosis Index entries containing back-references to D58.1:
  • Disease, diseased - see also Syndrome
    • hemoglobin or Hb
      • C (Hb-C) D58.2
        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)
        • elliptocytosis D58.1
      • elliptocytosis D58.1
  • Dresbach's syndrome D58.1 (elliptocytosis)
  • Elliptocytosis (congenital) (hereditary) D58.1
    • Hb C D58.1 (disease)
    • hemoglobin disease D58.1
  • Syndrome - see also Disease
    • Dresbach's D58.1 (elliptocytosis)

ICD-10-CM Codes Adjacent To D58.1
D57.412 Sickle-cell thalassemia with splenic sequestration
D57.419 …… unspecified
D57.8 Other sickle-cell disorders
D57.80 …… without crisis
D57.81 Other sickle-cell disorders with crisis
D57.811 Other sickle-cell disorders with acute chest syndrome
D57.812 Other sickle-cell disorders with splenic sequestration
D57.819 …… unspecified
D58 Other hereditary hemolytic anemias
D58.0 Hereditary spherocytosis
D58.1 Hereditary elliptocytosis
D58.2 Other hemoglobinopathies
D58.8 Other specified hereditary hemolytic anemias
D58.9 Hereditary hemolytic anemia, unspecified
D59 Acquired hemolytic anemia
D59.0 Drug-induced autoimmune hemolytic anemia
D59.1 Other autoimmune hemolytic anemias
D59.2 Drug-induced nonautoimmune hemolytic anemia
D59.3 Hemolytic-uremic syndrome
D59.4 Other nonautoimmune hemolytic anemias
D59.5 Paroxysmal nocturnal hemoglobinuria [Marchiafava-Micheli]

Reimbursement claims with a date of service on or after October 1, 2015 require the use of ICD-10-CM codes.