ICD-10 code D57 for Sickle-cell disorders is a medical classification as listed by WHO under the range - Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism .
V78. 2 - Screening for sickle-cell disease or trait | ICD-10-CM.
8: Other specified disorders of skin and subcutaneous tissue.
K31. 89 - Other diseases of stomach and duodenum. ICD-10-CM.
9: Fever, unspecified.
9.
L90. 8 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 L90.
The 2022 edition of ICD-10-CM L27. 8 became effective on October 1, 2021. This is the American ICD-10-CM version of L27.
ICD-10 code R10. 9 for Unspecified abdominal pain is a medical classification as listed by WHO under the range - Symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified .
Gastroptosis is the abnormal downward displacement of the stomach. Although this condition is not life threatening is associated with constipation, discomfort, vomiting, dyspepsia, tenesmus, anorexia, nausea and belching.
Code D64. 9 is the diagnosis code used for Anemia, Unspecified, it falls under the category of diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism. Anemia specifically, is a condition in which the number of red blood cells is below normal.
Other diseases of stomach and duodenum The 2022 edition of ICD-10-CM K31. 89 became effective on October 1, 2021.
ICD-10 Code for Local infection of the skin and subcutaneous tissue, unspecified- L08. 9- Codify by AAPC.
ICD-10 code: L98. 9 Disorder of skin and subcutaneous tissue, unspecified.
ICD-10-CM Code for Disorder of the skin and subcutaneous tissue, unspecified L98. 9.
A blood disorder characterized by the appearance of sickle-shaped red blood cells and anemia. A disease characterized by chronic hemolytic anemia, episodic painful crises, and pathologic involvement of many organs. It is the clinical expression of homozygosity for hemoglobin s.
Sickle cell anemia is caused by a mutation (change) in one of the genes for hemoglobin (the substance inside red blood cells that binds to oxygen and carries it from the lungs to the tissues). It is most common in people of west and central african descent.
The sickle cells also get stuck in blood vessels, blocking blood flow. This can cause pain and organ damage. A genetic problem causes sickle cell anemia. People with the disease are born with two sickle cell genes, one from each parent. If you only have one sickle cell gene, it's called sickle cell trait.