ICD-10-CM CATEGORY CODE RANGE SPECIFIC CONDITION ICD-10 CODE Diseases of the Circulatory System I00 –I99 Essential hypertension I10 Unspecified atrial fibrillation I48.91 Diseases of the Respiratory System J00 –J99 Acute pharyngitis, NOS J02.9 Acute upper respiratory infection J06._ Acute bronchitis, *,unspecified J20.9 Vasomotor rhinitis J30.0
Search the full ICD-10 catalog by:
ICD-10-CM Diagnosis Codes
| A00.0 | B99.9 | 1. Certain infectious and parasitic dise ... |
| C00.0 | D49.9 | 2. Neoplasms (C00-D49) |
| D50.0 | D89.9 | 3. Diseases of the blood and blood-formi ... |
| E00.0 | E89.89 | 4. Endocrine, nutritional and metabolic ... |
| F01.50 | F99 | 5. Mental, Behavioral and Neurodevelopme ... |
The ICD-10-CM is a catalog of diagnosis codes used by medical professionals for medical coding and reporting in health care settings. The Centers for Medicare and Medicaid Services (CMS) maintain the catalog in the U.S. releasing yearly updates.
Disorder of iron metabolism, unspecified E83. 10 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 E83. 10 became effective on October 1, 2021.
What: hemochromatosis: hemochromatosis: a disorder of iron metabolism characterized by excess deposition of iron in the tissues, especially the liver. It is characterized by pigmentation of the skin, hepatic cirrhosis, decreased carbohydrate tolerance, cardiomyopathy and endocrinopathy (especially hypogonadism).
ICD-10 code R68. 89 for Other general symptoms and signs is a medical classification as listed by WHO under the range - Symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified .
E83. 110 - Hereditary hemochromatosis | ICD-10-CM.
Hemosiderosis often results from multiple blood transfusions. Hemochromatosis refers to iron deposition in the parenchymal cells of the liver, pancreas, heart, and other organs. Hemochromatosis has greater clinical significance because it leads to cirrhosis and hepatocellular carcinoma.
Hemochromatosis has been separated into four distinct disorders – hereditary (classic) hemochromatosis, also known as HFE-related hemochromatosis or hemochromatosis type I, hemochromatosis type 2 (juvenile hemochromatosis), hemochromatosis type 3, also known as TFR-related hemochromatosis; and hemochromatosis type 4, ...
R68. 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 R68. 89 became effective on October 1, 2021.
ICD-10 code Z00. 01 for Encounter for general adult medical examination with abnormal findings is a medical classification as listed by WHO under the range - Factors influencing health status and contact with health services .
From ICD-10: For encounters for routine laboratory/radiology testing in the absence of any signs, symptoms, or associated diagnosis, assign Z01. 89, Encounter for other specified special examinations.
ICD-10 code E83. 11 for Hemochromatosis is a medical classification as listed by WHO under the range - Endocrine, nutritional and metabolic diseases .
Compound heterozygous (C282Y/H631) individuals may develop increased iron overload and are at increased risk of developing hemochromatosis. Figure 9. Chromosome 6, the H63D gene and the locus of the H63D mutation. A subgroup of patients with clinical HH does not have mutations in the HFE gene.
110.
What: hemochromatosis: hemochromatosis: a disorder of iron metabolism characterized by excess deposition of iron in the tissues, especially the liver. It is characterized by pigmentation of the skin, hepatic cirrhosis, decreased carbohydrate tolerance, cardiomyopathy and endocrinopathy (especially hypogonadism).
Idiopathic or genetic hemochromatosis is an autosomal recessive disorder of metabolism associated with a gene tightly linked to the a locus of the hla complex on chromosome 6. (from Dorland, 27th ed) An inherited metabolic disorder characterized by iron accumulation in the tissues.
A disorder due to the deposition of hemosiderin in the parenchymal cells, causing tissue damage and dysfunction of the liver, pancreas, heart, and pituitary. Full development of the disease in women is restricted by menstruation, pregnancy, and lower dietary intake of iron.
Condition in which there is a deviation or interruption in the storage of iron in the body. Hemochromatosis is an inherited disease in which too much iron builds up in your body. It is one of the most common genetic diseases in the United States. iron is a mineral found in many foods.
Idiopathic or genetic hemochromatosis is an autosomal recessive disorder of metabolism associated with a gene tightly linked to the a locus of the hla complex on chromosome 6. (from Dorland, 27th ed) An inherited metabolic disorder characterized by iron accumulation in the tissues.
A disorder due to the deposition of hemosiderin in the parenchymal cells, causing tissue damage and dysfunction of the liver, pancreas, heart, and pituitary. Full development of the disease in women is restricted by menstruation, pregnancy, and lower dietary intake of iron.
The ICD-10-CM Alphabetical Index links the below-listed medical terms to the ICD code E83.118. Click on any term below to browse the alphabetical index.
This is the official approximate match mapping between ICD9 and ICD10, as provided by the General Equivalency mapping crosswalk. This means that while there is no exact mapping between this ICD10 code E83.118 and a single ICD9 code, 275.03 is an approximate match for comparison and conversion purposes.