icd 10 code for alpha 1 antitrypsin deficiency

What is the ICD 10 code for antitrypsin deficiency?

Oct 01, 2021 · 2022 ICD-10-CM Diagnosis Code E88.01 Alpha-1-antitrypsin deficiency 2016 2017 2018 2019 2020 2021 2022 Billable/Specific Code E88.01 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 E88.01 became effective on October 1, 2021.

What is the ICD 10 code for alpha 1 deficiency?

E88.01 is a billable diagnosis code used to specify a medical diagnosis of alpha-1-antitrypsin deficiency. The code E88.01 is valid during the fiscal year 2022 from October 01, 2021 through September 30, 2022 for the submission of HIPAA-covered transactions. The ICD-10-CM code E88.01 might also be used to specify conditions or terms like alpha-1-antitrypsin deficiency, …

What is alpha-1-antitrypsin deficiency?

ICD-10-CM Code E88.01 Alpha-1-antitrypsin deficiency BILLABLE | ICD-10 from 2011 - 2016 E88.01 is a billable ICD code used to specify a diagnosis of alpha-1-antitrypsin deficiency. A 'billable code' is detailed enough to be used to specify a medical diagnosis. The ICD code E880 is used to code Alpha 1-antitrypsin deficiency

What is the ICD 10 code for encephalomyelitis?

ICD-10-CM Diagnosis Code E88.01 [convert to ICD-9-CM] Alpha - 1 - antitrypsin deficiency. Alpha 1 antitrypsin deficiency; AAT deficiency. ICD-10-CM Diagnosis Code E88.01. Alpha-1-antitrypsin deficiency. 2016 2017 2018 2019 2020 2021 2022 Billable/Specific Code. Applicable To.

What is alpha one antitrypsin?

Alpha-1-antitrypsin (AAT) is a protein produced in the liver that protects the body's tissues from being damaged by infection-fighting agents released by its immune system. In alpha-1 antitrypsin deficiency, the body's normal production of AAT is reduced, resulting in the destruction of sensitive lung tissue.Mar 24, 2020

Is there another name for alpha-1 antitrypsin deficiency?

Alpha-1 antitrypsin deficiency is a genetic disease, which means it's passed down to you from your parents. It can cause serious lung or liver disease. You may also hear it called AAT deficiency.Nov 17, 2019

What disease is caused by an alpha-1 antitrypsin deficiency?

Alpha-1 antitrypsin deficiency-associated lung disease is characterized by progressive degenerative and destructive changes in the lungs (emphysema, commonly of the panacinar type). Emphysema is a chronic, usually slowly progressive illness, which most commonly causes shortness of breath.

Is alpha-1 antitrypsin deficiency a blood disorder?

Alpha-1 is a rare genetic (inherited) disorder in which people have low levels of AAT in their bloodstream. This disorder can increase your risk of developing lung and liver diseases, including emphysema (damaged air sacs in the lungs) and cirrhosis (liver scarring).Dec 24, 2019

How do you know if you have alpha-1 antitrypsin deficiency?

When the liver is affected by AAT deficiency, symptoms may include tiredness, loss of appetite, weight loss, swelling of the feet or belly, yellowish discoloration of the skin (jaundice) or white part of the eyes, vomiting of blood, or blood in stools.Mar 24, 2020

What are the complications of alpha-1 antitrypsin deficiency?

Alpha-1 antitrypsin deficiency can cause various medical complications of the lungs, liver, and skin, including COPD, emphysema, chronic bronchitis, cirrhosis of the liver, panniculitis (inflammation of fatty tissue under the skin) and other side effects of the excess enzyme.

What is the diagnostic significance of α 1 antitrypsin?

This test measures the amount of alpha-1 antitrypsin (AAT) in the blood. AAT is a protein that is made in the liver. It helps protect your lungs from damage and diseases, such as emphysema and chronic obstructive pulmonary disease (COPD).Sep 13, 2021

Why does a1 antitrypsin destroy lungs?

Alpha-1 antitrypsin deficiency (AATD) is an inherited disorder characterized by low serum levels of alpha-1 antitrypsin (AAT). Loss of AAT disrupts the protease-antiprotease balance in the lungs, allowing proteases, specifically neutrophil elastase, to act uninhibited and destroy lung matrix and alveolar structures.

What is AAT deficiency?

Information for Patients. Alpha-1 antitrypsin deficiency (AAT deficiency) is an inherited condition that raises your risk for lung and liver disease. Alpha-1 antitrypsin (AAT) is a protein that protects the lungs.

When do you start to feel the symptoms of alpha 1?

The signs and symptoms of the condition and the age at which they appear vary among individuals.People with alpha-1 antitrypsin deficiency usually develop the first signs and symptoms of lung disease between ages 20 and 50. The earliest symptoms are shortness of breath following mild activity, reduced ability to exercise, and wheezing.

What is the AAT protein?

Alpha-1 antitrypsin (AAT) is a protein that protects the lungs. The liver makes it. If the AAT proteins aren't the right shape, they get stuck in the liver cells and can't reach the lungs. Symptoms of AAT deficiency include.

What are the symptoms of cirrhosis?

Signs of cirrhosis include a swollen abdomen, swollen feet or legs, and jaundice. Individuals with alpha-1 antitrypsin deficiency are also at risk of developing a type of liver cancer called hepatocellular carcinoma.In rare cases, people with alpha-1 antitrypsin deficiency develop a skin condition called panniculitis, ...

What is the E88.01 code?

E88.01 is a billable diagnosis code used to specify a medical diagnosis of alpha-1-antitrypsin deficiency. The code E88.01 is valid during the fiscal year 2021 from October 01, 2020 through September 30, 2021 for the submission of HIPAA-covered transactions.

What are the symptoms of emphysema?

Other signs and symptoms can include unintentional weight loss, recurring respiratory infections, fatigue, and rapid heartbeat upon standing. Affected individuals often develop emphysema, which is a lung disease caused by damage to the small air sacs in the lungs (alveoli).

Does smoking cause emphysema?

Smoking or exposure to tobacco smoke accelerates the appearance of emphysema symptoms and damage to the lungs. About 10 percent of infants with alpha-1 antitrypsin deficiency develop liver disease, which often causes yellowing of the skin and whites of the eyes (jaundice).

What is the A1AT gene?

Alpha 1-antitrypsin deficiency (α1-antitrypsin deficiency, A1AD) is a genetic disorder that causes defective production of alpha 1-antitrypsin (A1AT), leading to decreased A1AT activity in the blood and lungs, and deposition of excessive abnormal A1AT protein in liver cells. There are several forms and degrees of deficiency; the form and degree depend on whether the sufferer has one or two copies of the defective allele because it is a co-dominant trait. Severe A1AT deficiency causes panacinar emphysema or COPD in adult life in many people with the condition (especially if they are exposed to cigarette smoke). The disorder can lead to various liver diseases in a minority of children and adults, and occasionally more unusual problems. It is treated through avoidance of damaging inhalants and, in severe cases, by intravenous infusions of the A1AT protein or by transplantation of the liver or lungs. It usually produces some degree of disability and reduces life expectancy.

How is A1AT treated?

It is treated through avoidance of damaging inhalants and, in severe cases, by intravenous infusions of the A1AT protein or by transplantation of the liver or lungs. It usually produces some degree of disability and reduces life expectancy. Specialty: Pulmonology, Medical Genetics. MeSH Code:

What is inclusion term?

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.