To view other topics, please sign in or purchase a subscription.. ICD-10-CM 2021 Coding Guide™ from Unbound Medicine. Search online 72,000+ ICD-10 codes by number, disease, injury, drug, or keyword. 282.0 - Hereditary spherocytosis is a topic covered in the ICD-10-CM.. To view the entire topic, please sign in or purchase a subscription..
This is the American ICD-10-CM version of D58.9 - other international versions of ICD-10 D58.9 may differ. ICD-10-CM Diagnosis Codes D58.0 - Hereditary spherocytosis The above description is abbreviated. This code description may also have Includes, Excludes, Notes, Guidelines, Examples and other information. 2018-06-19 · Hereditary spherocytosis may be caused by changes (mutations) in any of several genes. These genes give the body instructions to make proteins that exist on the membranes of red blood cells .
Centers for Medicare and Medicaid Services and the National Center for Health Statistics; 2018. [cited 2021 February 10]. Available from: https://www.unboundmedicine.com/icd/view/ICD-10-CM/861208/all/D58_0___Hereditary_spherocytosis.
D58.0 is a VALID/BILLABLE ICD10 code, i.e it is valid for submission for HIPAA-covered transactions.
Acholuric (familial)
Aug 9, 2012 ICD-10 Chapter D · 1 C00-D48 - Neoplasms. 1.1 (C00-C14) Malignant neoplasms, lip, oral cavity and pharynx; 1.2 (C15-C26) Malignant
Aug 18, 2020 Hereditary spherocytosis is a condition that affects red blood cells. have the moderate form, 10 percent have the moderate/severe form, and 3
Mar 23, 2021 Section 41515.2: Infectious Diseases (ICD-10 A00-B99) congenital spherocytosis, sickle cell disease, the thalassemias and erythroblastosis
Hereditary spherocytosis D50-D89 2021 ICD-10-CM Range D50-D89 Diseases of the blood and blood-forming organs and certain disorders involving the D58 ICD-10-CM Diagnosis Code D58 Other hereditary hemolytic anemias 2016 2017 2018 2019 2020 2021
Hereditary spherocytosis Valid for Submission. D58.0 is a billable diagnosis code used to specify a medical diagnosis of hereditary spherocytosis. Code Classification.
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Hereditary spherocytosis · D58.0 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. · The 2021 edition of Revised the PDPM SLP comorbidity to ICD-10-CM mapping by adding more speech related 6756, D580, Hereditary spherocytosis, Medical Management, N /A. Sickle-cell trait (D57.3). Other sickle-cell disorders (D57.8). Other hereditary hemolytic anemias (D58).
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. For claims with a date of service on or after October 1, 2015, use an equivalent ICD-10-CM code (or codes).
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- splenic D64.89. - splenomegalic D64.89. - stomatocytosis D58.8.
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A) D58.0 B) D58.00 C) D58.09 D) D58.2 Hereditary spherocytosis. ICD-10-CM D58.0. https://icd10coded.com/cm/D58.0/. Includes: Acholuric (familial) jaundice, Congenital (spherocytic) hemolytic icterus, Minkowski-Chauffard syndrome. Index of diseases: Spherocytosis (congenital) (familial) (hereditary) ← Previous. Page 1. Next Page →.
Applicable To. Acholuric (familial) jaundice. Congenital (spherocytic) hemolytic icterus. Minkowski-Chauffard syndrome. sickle-cell D57.8- (disease) ICD-10-CM Diagnosis Code D57.8-. Research Hospitalization Volume, DRGs, Quality Outcomes, Top Hospitals & Physicians for D580 - Hereditary spherocytosis - ICD 10 Diagnosis Code References in the ICD-10-CM Index to Diseases and Injuries applicable to the clinical term spherocytosis (congenital) (familial) (hereditary) 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.
- syphilitic (acquired) (late) A52.79 [D63.8]. Hereditary spherocytosis · D58.0 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. · The 2021 edition of Revised the PDPM SLP comorbidity to ICD-10-CM mapping by adding more speech related 6756, D580, Hereditary spherocytosis, Medical Management, N /A. Sickle-cell trait (D57.3).