Search results for “Noonan's syndrome”. Diagnosis Code Q871 Billable Congenital malformations, deformations and chromosomal abnormalities / Other congenital malformations / Other specified congenital malformation syndromes affecting multiple systems.
Z77-Z99 2019 ICD-10-CM Range Z77-Z99. Persons with potential health hazards related to family and personal history and certain conditions influencing health status Code Also any follow-up examination (Z08-Z09) Persons with potential health hazards related to family and personal history and certain conditions influencing health status.
Z83.49 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. Short description: Family history of endo, nutritional and metabolic diseases. The 2019 edition of ICD-10-CM Z83.49 became effective on October 1, 2018.
Family history of other mental and behavioral disorders. Z81.8 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
"Q87. 19 - Other Congenital Malformation Syndromes Predominantly Associated With Short Stature." ICD-10-CM, 10th ed., Centers for Medicare and Medicaid Services and the National Center for Health Statistics, 2018.
Family history of other specified conditions Z84. 89 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 Z84. 89 became effective on October 1, 2021.
ICD-10 Code for Family history of carrier of genetic disease- Z84. 81- Codify by AAPC. Factors influencing health status and contact with health services. Persons with potential health hazards related to family and personal history and certain conditions influencing health status.
ICD-10 Code for Headache, unspecified- R51. 9- Codify by AAPC.
Z83.42Z83. 42 - Family history of familial hypercholesterolemia. ICD-10-CM.
ICD-10 code Z82. 3 for Family history of stroke is a medical classification as listed by WHO under the range - Factors influencing health status and contact with health services .
Mutations in the MUTYH gene cause an autosomal recessive form of familial adenomatous polyposis (also called MUTYH-associated polyposis). Mutations in this gene affect the ability of cells to correct errors made during DNA replication.
Mutations in the BRCA2 gene are associated with an increased risk of breast cancer in both men and women, as well as several other types of cancer. These mutations are present in every cell in the body and can be passed from one generation to the next.
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.
S09. 90XA Unspecified injury of head, initial encounter - ICD-10-CM Diagnosis Codes.
Code R53. 83 is the diagnosis code used for Other Fatigue. It is a condition marked by drowsiness and an unusual lack of energy and mental alertness. It can be caused by many things, including illness, injury, or drugs.
ICD-10 code G89. 29 for Other chronic pain is a medical classification as listed by WHO under the range - Diseases of the nervous system .