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ICD-10-CM Code D58.0
Hereditary spherocytosis

Billable Code
Billable codes are sufficient justification for admission to an acute care hospital when used a principal diagnosis.
| ICD-10 from 2011 - 2016

D58.0 is a billable ICD code used to specify a diagnosis of hereditary spherocytosis. A 'billable code' is detailed enough to be used to specify a medical diagnosis.

The ICD code D580 is used to code Hereditary spherocytosis

Hereditary spherocytosis (also known as Minkowski–Chauffard syndrome) is an autosomal dominant abnormality of erythrocytes. The disorder is caused by mutations in genes relating to membrane proteins that allow for the erythrocytes to change shape. The abnormal erythrocytes are sphere-shaped (spherocytosis) rather than the normal biconcave disk shaped. Dysfunctional membrane proteins interfere with the cell's ability to be flexible to travel from the arteries to the smaller capillaries. This difference in shape also makes the red blood cells more prone to rupture. Cells with these dysfunctional proteins are taken for degradation at the spleen. This shortage of erythrocytes results in hemolytic anemia.

Specialty: Hematology
MeSH Code: D013103
ICD 9 Code: 282.0

Peripheral blood smear from patient with hereditary spherocytosis

Source: Wikipedia

Coding Notes for D58.0 Info for medical coders on how to properly use this ICD-10 code

Inclusion Terms:
Inclusion Terms
Inclusion Terms are a list of concepts for which a specific code is used. The list of Inclusion Terms is useful for determining the correct code in some cases, but the list is not necessarily exhaustive.
Acholuric (familial) jaundice
Congenital (spherocytic) hemolytic icterus
Minkowski-Chauffard syndrome

MS-DRG Mapping

  • DRG Group #811-812 - Red blood cell disorders with MCC.
  • DRG Group #811-812 - Red blood cell disorders without MCC.

ICD-10-CM Alphabetical Index References for 'D58.0 - Hereditary spherocytosis'

The ICD-10-CM Alphabetical Index links the below-listed medical terms to the ICD code D58.0. Click on any term below to browse the alphabetical index.

Spherocytosis(congenital) (familial) (hereditary) (D58.0)


Hereditary spherocytosis (exact match)

This is the official exact match mapping between ICD9 and ICD10, as provided by the General Equivalency mapping crosswalk. This means that in all cases where the ICD9 code 282.0 was previously used, D58.0 is the appropriate modern ICD10 code.

Parent Code: D58 - Other hereditary hemolytic anemias

** This Document Provided By ICD.Codes **
Source: http://icd.codes/icd10cm/D580