ICD-10-CM/PCS codes version 2016/2017/2018/2019/2020/2021, ICD10 data search engine

ICD-10 D58.0 is hereditary spherocytosis (D580). This code is grouped under diagnosis codes for diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism.

HEREDITARY. 0 - Hereditary spherocytosis. 1 - Hereditary elliptocytosis. 2 - Other hemoglobinopathies. May 9, 2019 Coding Policy Manual and Change Report (ICD-10-CM). *April 2021 Hereditary nephropathy, not elsewhere classified with unspecified morphologic lesions poisoning, arsenic poisoning, and spherocytosis. 7.

D582. ENZYME DISORDERS. D55. Other Hemolytic Anemias. HEREDITARY. 0 - Hereditary spherocytosis.

ICD-10-CM Diagnosis Code D58.0 [convert to ICD-9-CM] Hereditary spherocytosis. Spherocytosis, hereditary; Acholuric (familial) jaundice; Congenital (spherocytic) hemolytic icterus; Minkowski-Chauffard syndrome. ICD-10-CM Diagnosis Code D58.0. Hereditary spherocytosis.

ICD-10-CM Diagnosis Code D58.0. Hereditary spherocytosis.

Related 2021 ICD-10-CM Codes to D58.0 Hereditary spherocytosis. ICD-10-CM Index; Chapter: D50–D89; Section: D55-D59; Block: D58; D58.0 - Hereditary spherocytosis

This code description may also have Includes, Excludes, Notes, Guidelines, Examples and other information. Access to this feature is available in the following products: Find-A-Code Essentials. HCC Plus. D58.0 - Hereditary spherocytosis answers are found in the ICD-10-CM powered by Unbound Medicine.

Hereditary spherocytosis ICD-9-CM 282.0 is a billable medical code that can be used to indicate a diagnosis on a reimbursement claim, however, 282.0 should only be used for claims with a date of service on or before September 30, 2015. The ICD-10-CM Alphabetical Index is designed to allow medical coders to look up various medical terms and connect them with the appropriate ICD codes. There are 2 terms under the parent term 'Spherocytosis' in the ICD-10-CM Alphabetical Index.
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Legacy ICD-9-CM Codes.

D57.01 Hb-SS disease with acute chest syndrome.
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ENZYME DISORDERS. D55. Other Hemolytic Anemias. HEREDITARY. 0 - Hereditary spherocytosis. 1 - Hereditary elliptocytosis. 2 - Other hemoglobinopathies.

ICD-10 D58.0 is hereditary spherocytosis (D580). This code is grouped under diagnosis codes for diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism.

Hereditary spherocytosis D58.0. The ICD10 code for the diagnosis "Hereditary spherocytosis" is "D58.0". D58.0 is a VALID/BILLABLE ICD10 code, i.e it is valid for submission for HIPAA-covered transactions. D58.0 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.

This code description may also have Includes, Excludes, Notes, Guidelines, Examples and other information. Hereditary spherocytosis is an abnormality of red blood cells, or erythrocytes. A chronic disease with a long term health condition with no cure. The disorder is caused by mutations in genes relating to membrane proteins that allow for the erythrocytes to change shape.

There are 2 terms under the parent term 'Spherocytosis' in the ICD-10-CM Alphabetical Index. Hereditary spherocytosis ICD-9-CM 282.0 is a billable medical code that can be used to indicate a diagnosis on a reimbursement claim, however, 282.0 should only be used for claims with a date of service on or before September 30, 2015. ICD-10 D58.0 is hereditary spherocytosis (D580). This code is grouped under diagnosis codes for diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism. Medical search and APIs for ICD10, SNOMED, LOINC, NPIs and much more by 1upHealth. Elliptocytosis (congenital) Ovalocytosis (congenital) (hereditary) ICD-10-CM Diagnosis Code E83.110 [convert to ICD-9-CM] Hereditary hemochromatosis.