icd 10 code for cftr mutation

Full Answer

What is the ICD 10 code for genetic carrier of other disease?

Genetic carrier of other disease. Z14.8 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.

What is the ICD 10 code for uremia?

E84.9 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. The 2019 edition of ICD-10-CM E84.9 became effective on October 1, 2018. This is the American ICD-10-CM version of E84.9 - other international versions of ICD-10 E84.9 may differ.

What is the DX code for MLH1 gene mutation?

Gene Mutation dx codes 1 MLH1 gene mutation (V84.89) (Z15.89) 2 Genetic predisposition to cancer (V84.09) (Z15.09) More ...

What is the ICD-10 code for gene mutation?

Chromosomal abnormality, unspecified Q99. 9 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 Q99. 9 became effective on October 1, 2021.

What is the ICD code for cystic fibrosis?

Code E84. 8 is for cystic fibrosis with other manifestations, and code E84. 9 is assigned for unspecified cystic fibrosis.

What is the ICD-10 code for cystic fibrosis exacerbation?

0.

What is the ICD-10 code for genetic disease carrier?

ICD-10 code Z14. 8 for Genetic carrier of other disease is a medical classification as listed by WHO under the range - Factors influencing health status and contact with health services .

What type of mutation is CFTR?

There are five classes of CFTR mutations: protein production, protein processing, gating, conduction, and insufficient protein. The most common CF mutation, F508del, is primarily considered to be a protein processing mutation. CFTR modulators address various problems caused by different types of CFTR mutations.

What is CFTR stand for?

The cystic fibrosis transmembrane conductance regulator ( CFTR The cystic fibrosis transmembrane conductance regulator (CFTR) protein is a chloride channel that is responsible for regulating the proper flow of chloride and sodium (components of salt) in and out of the cell membranes in the lungs and other organs. )

What is the ICD-10 code for post inflammatory pulmonary fibrosis?

515 - Postinflammatory pulmonary fibrosis | ICD-10-CM.

What are pulmonary manifestations of cystic fibrosis?

Early manifestations of the CF pulmonary phenotype include increased airway resistance, evidence of gas trapping and diminished expiratory flow rates and volumes. These abnormalities have been reported in young patients with mild CF (6) and in clinically stable individuals without detectable infection (7–14).

What is the ICD-10 code for Panhypopituitarism?

E23. 0 - Hypopituitarism. ICD-10-CM.

What are gene mutations?

A gene variant is a permanent change in the DNA sequence that makes up a gene. This type of genetic change used to be known as a gene mutation, but because changes in DNA do not always cause disease, it is thought that gene variant is a more accurate term.

What is the ATM gene mutation?

Researchers have identified several hundred mutations in the ATM gene that cause ataxia-telangiectasia. People with this disorder have mutations in both copies of the ATM gene in each cell. Most of these mutations disrupt protein production, resulting in an abnormally small, nonfunctional version of the ATM protein.

What is the ICD-10 code for sickle cell trait?

ICD-10-CM Code for Sickle-cell trait D57. 3.

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