The lack of sufficient energy or protein to meet the body's metabolic demands, as a result of either an inadequate dietary intake of protein, intake of poor quality dietary protein, increased demands due to disease, or increased nutrient losses. ICD-10-CM E46 is grouped within Diagnostic Related Group (s) (MS-DRG v38.0):
O99- Other maternal diseases classifiable elsewhere but complicating pregnancy, childbirth and the puerperium 2021 ICD-10-CM Diagnosis Code O99.280 O99.280 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. The 2021 edition of ICD-10-CM O99.280 became effective on October 1, 2020.
Unspecified protein-calorie malnutrition. E46 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
Endocrine, nutritional and metabolic diseases complicating pregnancy, unspecified trimester 2016 2017 2018 2019 2020 2021 Billable/Specific Code Maternity Dx (12-55 years) O99.280 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
ICD-10 code Z71. 89 for Other specified counseling is a medical classification as listed by WHO under the range - Factors influencing health status and contact with health services .
D68. 2 - Hereditary deficiency of other clotting factors. ICD-10-CM.
Inheritance. Protein S deficiency is inherited in an autosomal dominant pattern , which means one altered copy of the PROS1 gene in each cell is sufficient to cause mild protein S deficiency. Individuals who inherit two altered copies of this gene in each cell have severe protein S deficiency.
The 2022 edition of ICD-10-CM Z76. 0 became effective on October 1, 2021. This is the American ICD-10-CM version of Z76.
Acquired factor VII deficiency can result from severe liver disease, sepsis or vitamin K deficiency. Certain drugs such as warfarin (CoumadinĀ®) can result in acquired factor VII deficiency. Acquired factor VII deficiency is more common than the inherited form.
Factor VII, also called proconvertin, is one such clotting factor produced by the liver. It requires vitamin K for its production. Along with other clotting factors and blood cells, it promotes blood clotting at the site of an injury. It forms normal blood clots and closes the wound to prevent blood loss.
Protein S deficiency is a rare inherited thrombophilia often associated with fetal losses in pregnancy. It is seen in approximately 1 in 500 to 1 in 3,000 people. Homozygous Protein S deficiency in neonates manifests as a catastrophic and fatal thrombotic complication termed Purpura Fulminans (PF).
Protein S is a vitamin Kādependent anticoagulant protein that was first discovered in Seattle, Washington in 1979 and arbitrarily named after that city.
Congenital C and S proteins are natural substances in the blood that help prevent blood clots. Protein C deficiency occurs in approximately 1 of every 200 to 500 people, whereas protein S deficiency occurs in approximately 1 of every 500 individuals.1,2 Deficiency may be determined from a blood sample.
E63.9ICD-10 code E63. 9 for Nutritional deficiency, unspecified is a medical classification as listed by WHO under the range - Endocrine, nutritional and metabolic diseases .
E40-E46 - Malnutrition. ICD-10-CM.
Dietary counseling and surveillanceICD-10 code Z71. 3 for Dietary counseling and surveillance is a medical classification as listed by WHO under the range - Factors influencing health status and contact with health services .