icd 10 code for hereditary spherocytosis

What is heredity spherocytosis?

Oct 01, 2021 · Hereditary spherocytosis. D58.0 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. The 2022 edition of ICD-10-CM D58.0 became effective on October 1, 2021. This is the American ICD-10-CM version of D58.0 - other international versions of ICD-10 D58.0 may differ.

What is the ICD 10 code for Minkowski-Chauffard syndrome?

Hereditary spherocytosis (D58.0) D58 D58.0 D58.1 ICD-10-CM Code for Hereditary spherocytosis D58.0 ICD-10 code D58.0 for Hereditary spherocytosis is a medical classification as listed by WHO under the range - Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism .

What is the ICD 10 code for hemolytic anemia?

ICD-10-CM Code D58.0 Hereditary spherocytosis BILLABLE | 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

What does hereditary spherocytosis mean?

Hereditary spherocytosis is a condition that affects red blood cells. People with this condition typically experience a shortage of red blood cells (anemia ), yellowing of the eyes and skin (jaundice), and an enlarged spleen (splenomegaly).

What is the diagnosis for hereditary spherocytosis?

Hereditary spherocytosis was diagnosed on the basis of clinical and laboratory signs of chronic hemolysis, presence of spherocytes at peripheral blood smear examination, positivity of at least one red cell fragility test, family history of hereditary spherocytosis if any, and exclusion of other causes of secondary ...

What type of anemia is hereditary spherocytosis?

Hereditary spherocytosis is a condition characterized by hemolytic anemia (when red blood cells are destroyed earlier than normal). Signs and symptoms can range from mild to severe and may include pale skin, fatigue, anemia , jaundice , gallstones, and/or enlargement of the spleen.

Where is defect in hereditary spherocytosis?

Hereditary spherocytosis (HS) is a familial hemolytic disorder associated with a variety of mutations that lead to defects in red blood cell (RBC) membrane proteins. It is also one of the most common causes of hemolytic anemia due to membrane defect.Feb 18, 2021

What are the classic laboratory findings of hereditary spherocytosis?

The classic laboratory features of HS include the following [3, 4] : Mild to moderate anemia. Reticulocytosis. Increased MCHC.

What are the clinical features of hereditary spherocytosis?

Hereditary spherocytosis (HS) is an inherited disease that affects the red blood cells. Characteristic symptoms of HS are the destruction of red blood cells in the spleen and their removal from the blood stream (hemolytic anemia), a yellow tone to the skin (jaundice), and an enlarged spleen (splenomegaly).

Is hereditary spherocytosis Hyperchromic?

The arrows point to spherocytes, correctly identified by 97.3% of the participants. Spherocytes are erythrocytes that are hyperchromic and lack central pallor due to their spherical shape. This contrasts with normal erythrocytes, which have a biconcave shape and visible central pallor on smear preparations.

Can you give blood if you have hereditary spherocytosis?

1. Must not donate if: Clinically significant haemolysis.

What is EMA binding test?

Background: The eosin-5′-maleimide (EMA) binding test is a flow cytometric test widely used to detect hereditary spherocytosis (HS). EMA binds to plasma membrane proteins of red blood cells (RBCs), mainly to band 3 protein.

What gene mutation causes hereditary spherocytosis?

About half of all cases of hereditary spherocytosis are due to mutations in the ANK1 gene. Other genes associated with the condition include the EPB42, SLC4A1, SPTA1, and SPTB genes.

Why is MCHC high in hereditary spherocytosis?

MCHC values greater than the upper limit of normal (35-36%) are common. This increased MCHC is a result of mild cellular dehydration. The mean cell volume (MCV) in patients with HS actually is low, presumably because of membrane loss and cell dehydration.Feb 18, 2021

Why does splenomegaly occur in hereditary spherocytosis?

Doctors may refer to an enlarged spleen as splenomegaly. In hereditary spherocytosis, red blood cells become trapped in the spleen faster than the spleen can destroy them. As a result, the spleen grows larger. As a result of this constant breakdown (hemolysis), the contents of red blood cells are released.Jan 2, 2019

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.

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

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.

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.

Equivalent ICD-9 Code GENERAL EQUIVALENCE MAPPINGS (GEM)

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.

What is the ICd 10 code for hereditary spherocytosis?

D58.0 is a billable diagnosis code used to specify a medical diagnosis of hereditary spherocytosis. The code D58.0 is valid during the fiscal year 2021 from October 01, 2020 through September 30, 2021 for the submission of HIPAA-covered transactions.#N#The ICD-10-CM code D58.0 might also be used to specify conditions or terms like anemia due to membrane defect, hereditary spherocytosis, hereditary spherocytosis due to beta spectrin defect, hereditary spherocytosis due to combined deficiency of spectrin and ankyrin, hereditary spherocytosis due to deficiency of protein 4.2 , hereditary spherocytosis due to spectrin deficiency, etc.

Why is my blood not carrying oxygen?

If you have anemia, your blood does not carry enough oxygen to the rest of your body. The most common cause of anemia is not having enough iron. Your body needs iron to make hemoglobin. Hemoglobin is an iron-rich protein that gives the red color to blood. It carries oxygen from the lungs to the rest of the body.