Hereditary spherocytosis Hereditary spherocytosisClassification & external resources ICD-10 D58.0 ICD-9 282.0 OMIM 182900 DiseasesDB 5827 eMedicine D58.1 is a valid billable ICD-10 diagnosis code for Hereditary elliptocytosis. It is found in the 2021 version of the ICD-10 Clinical Modification (CM) and can be used in all HIPAA-covered transactions from Oct 01, 2020 - Sep 30, 2021. ↓ See below for any exclusions, inclusions or special notations D58.1 also applies to the following: D58.0 - Hereditary spherocytosis is a sample topic from the ICD-10-CM.. To view other topics, please sign in or purchase a subscription..

D580. Hereditary spherocytosis. 3. D581. Hereditary elliptocytosis.

282.0 is a legacy non-billable code used to specify a medical diagnosis of hereditary spherocytosis. This code was replaced on September 30, 2015 by its ICD-10 equivalent. There are not any answers for this question yet.

2016 2017 2018 2019 2020 2021 Billable/Specific Code. Applicable To. Acholuric (familial) jaundice. Congenital (spherocytic) hemolytic icterus.

Spherocytosis, hereditary; Acholuric (familial) jaundice; Congenital (spherocytic) hemolytic icterus; Minkowski-Chauffard syndrome.

Hereditary elliptocytosis Feb 16, 2020 ICD-10-CM/PCS codes and include both current and obsolete codes. Hereditary spherocytosis" "D581 " = "D581 : Hereditary elliptocytosis" ICD-10 Codes Supporting Medical Necessity Numerical Listing for CPT Code 88182: Medicare Medical Necessity for Laboratory Testing.
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Hereditary spherocytosis is represented by which ICD-10-CM code? A) D58.0 B) D58.00 C) D58.09 D) D58.2 Hereditary spherocytosis. ICD-10-CM D58.0.

D599.
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The format is GTR00000001.1, with a leading prefix 'GTR' followed by 8 digits, a period, then 1 or more digits representing the version. Spherocytosis most often refers to hereditary spherocytosis. This is caused by a molecular defect in one or more of the proteins of the red blood cell cytoskeleton , including spectrin , ankyrin , Band 3 , or Protein 4.2 . D58.9 is a valid billable ICD-10 diagnosis code for Hereditary hemolytic anemia, unspecified.It is found in the 2021 version of the ICD-10 Clinical Modification (CM) and can be used in all HIPAA-covered transactions from Oct 01, 2020 - Sep 30, 2021. Hereditary spherocytosis: | | | Hereditary spherocytosis | | | | World Heritage Encyclopedia, the aggregation of the largest online encyclopedias available, and Hereditary spherocytosis is a condition that affects red blood cells. People with this condition typically experience a shortage of red blood cells (), yellowing of the eyes and skin (jaundice), and an enlarged spleen (splenomegaly). Hereditary spherocytosis is the most common congenital hemolytic anemia among Caucasians with an estimated prevalence ranging from 1:2,000 to 1:5,000.

Thi References in the ICD-10-CM Index to Diseases and Injuries applicable to the clinical term "spherocytosis (congenital) (familial) (hereditary)" Spherocytosis (congenital) (familial) (hereditary) - D58.0 Hereditary spherocytosis hemoglobin disease - D58.0 Hereditary spherocytosis sickle-cell (disease) - D57.8 Other sickle-cell disorders ICD-10-CM/PCS MS-DRG v37.0 Definitions Manual: Hereditary spherocytosis: D581: Hereditary elliptocytosis: Congenital and hereditary thrombocytopenia purpura: ICD-10-CM Diagnosis Codes. D58.0 - Hereditary spherocytosis. The above description is abbreviated.

The ICD code D580 is used to code Hereditary spherocytosis Se hela listan på icdlist.com ICD-10-CM Code. D58.0. Hereditary spherocytosis Billable Code. D58.0 is a valid billable ICD-10 diagnosis code for Hereditary spherocytosis . It is found in the 2021 version of the ICD-10 Clinical Modification (CM) and can be used in all HIPAA-covered transactions from Oct 01, 2020 - Sep 30, 2021 . ICD-10-CM Diagnosis Code D58.0. Hereditary spherocytosis.