icd 10 code for pten mutation

What are symptoms of PTEN?

PTEN is a gene that helps stop cells from replicating and growing out of control. ... and autism. Other signs and symptoms of this syndrome include weak muscle tone, scoliosis, seizures, and ...

What does the PTEN gene do?

• Multiple hamartomas, especially in the gastrointestinal area
• Macrocephaly (larger than normal sized head)
• Developmental delays
• Autism
• Dark freckling of the penis in males
• Breast cancer
• Thyroid cancer
• Uterine cancer in females

What is PTEN syndrome?

The PTEN hamartoma tumor syndrome (PHTS) is a spectrum of disorders caused by mutations of the PTEN tumor suppressor gene in egg or sperm cells (germline). These disorders are characterized by multiple hamartomas that can affect various areas of the body.

What is a PTEN mutation?

Phosphatase and tensin homolog ( PTEN) is a phosphatase, in humans, is encoded by the PTEN gene. Mutations of this gene are a step in the development of many cancers, specifically glioblastoma, lung cancer, breast cancer, and prostate cancer.

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-10 code for BRCA mutation?

Genetic susceptibility to malignant neoplasm of breast The 2022 edition of ICD-10-CM Z15. 01 became effective on October 1, 2021. This is the American ICD-10-CM version of Z15.

What is Z15 89 code?

ICD-10 code Z15. 89 for Genetic susceptibility to other disease is a medical classification as listed by WHO under the range - Factors influencing health status and contact with health services .

What is the diagnosis for code R46 89?

R46. 89 - Other Symptoms and Signs Involving Appearance and Behavior [Internet]. In: ICD-10-CM.

What is the ICD-10 code for BRCA2 gene mutation positive?

BRCA1 and/or 2 positive results are assigned either ICD-10-CM code Z15. 01 Genetic susceptibility to malignant neoplasm of breast or Z15. 02 Genetic susceptibility to malignant neoplasm of ovary, depending on family history.

What is code Z12 39?

39 (Encounter for other screening for malignant neoplasm of breast). Z12. 39 is the correct code to use when employing any other breast cancer screening technique (besides mammogram) and is generally used with breast MRIs.

What ICD-10 code covers HLA b27?

Ankylosing spondylitis of unspecified sites in spine The 2022 edition of ICD-10-CM M45. 9 became effective on October 1, 2021. This is the American ICD-10-CM version of M45.

What are gene mutations?

What Is a Gene Mutation? A gene mutation (myoo-TAY-shun) is a change in one or more genes. Some mutations can lead to genetic disorders or illnesses.

What is the ICD-10 code for global developmental delay?

Encounter for screening for global developmental delays (milestones) Z13. 42 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 altered mental status?

82 Altered mental status, unspecified.

What does anxiety F41 9 mean?

Code F41. 9 is the diagnosis code used for Anxiety Disorder, Unspecified. It is a category of psychiatric disorders which are characterized by anxious feelings or fear often accompanied by physical symptoms associated with anxiety.

What is the ICD-10 code for abnormal behavior?

2.

What is the ICd 10 code for genetic susceptibility?

Genetic susceptibility to other disease 1 Z15.89 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. 2 The 2021 edition of ICD-10-CM Z15.89 became effective on October 1, 2020. 3 This is the American ICD-10-CM version of Z15.89 - other international versions of ICD-10 Z15.89 may differ.

What is a Z00-Z99?

Categories Z00-Z99 are provided for occasions when circumstances other than a disease, injury or external cause classifiable to categories A00 -Y89 are recorded as 'diagnoses' or 'problems'. This can arise in two main ways:

What is the name of the disease that is caused by mutations in the PTEN gene?

Proteus-like syndrome - people with many of the signs and symptoms associated with Proteus syndrome, but who do not meet the diagnostic criteria. PTEN hamartoma tumor syndrome is caused by changes ( mutations) in the PTEN gene and is inherited in an autosomal dominant manner.

What is PTEN hamartoma?

PTEN hamartoma tumor syndrome refers to a spectrum of conditions that are characterized by multiple hamartomas. These conditions include: Cowden syndrome - associated with a high risk for benign and malignant (cancerous) tumors of the thyroid, breast, and uterus. Affected people may also have macrocephaly and characteristic skin abnormalities.