Methemoglobinemia, unspecified D74. 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 D74. 9 became effective on October 1, 2021.
Symptoms of methemoglobinemia may vary depending on which type you have. The main symptoms are: cyanosis, which describes a bluish color of the skin, especially the lips and fingers. chocolate-brown colored blood.
ICD-10 code R23. 0 for Cyanosis is a medical classification as listed by WHO under the range - Symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified .
ICD-10-CM Diagnosis Code D50 D50.
Autosomal recessive congenital methemoglobinemia is an inherited condition that mainly affects the function of red blood cells. Specifically, it alters a molecule within these cells called hemoglobin. Hemoglobin carries oxygen to cells and tissues throughout the body.
The most likely cause of methemoglobinemia, therefore, is acquired by exposure to prilocaine hydrochloride.
ICD-10 Code for Cyanotic attacks of newborn- P28. 2- Codify by AAPC.
R23. 0 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 R23.
Definition of cyanotic : marked by or causing a bluish or purplish discoloration (as of the skin and mucous membranes) due to deficient oxygenation of the blood : relating to or affected with cyanosis On arrival at the emergency room, the patient was cyanotic and unconscious with labored respirations at 40/min.—
Each type has its own causes. In microcytic anemia, red blood cells (RBCs) are smaller than normal. In macrocytic anemia, RBCs are larger than normal. Making this distinction in the size of RBCs will help doctors figure out the cause of a person's anemia.
What causes macrocytic anemia? People may develop macrocytic anemia when they don't get enough vitamin B12 and/or folate (vitamin B9) to create healthy red blood cells, or they have medical conditions that prevent their bodies from absorbing those nutrients.
ICD-Code I10 is a billable ICD-10 code used for healthcare diagnosis reimbursement of Essential (Primary) Hypertension.
Methemoglobinemia (or methaemoglobinaemia) is a disorder characterized by the presence of a higher than normal level of methemoglobin (metHb, i.e., ferric [Fe3+] rather than ferrous [Fe2+] haemoglobin) in the blood. Methemoglobin is a form of hemoglobin that contains ferric [Fe3+] iron and has a decreased ability to bind oxygen. However, the ferrous iron has an increased affinity for bound oxygen. The binding of oxygen to methemoglobin results in an increased affinity of oxygen to the three other heme sites (that are still ferrous) within the same tetrameric hemoglobin unit. This leads to an overall reduced ability of the red blood cell to release oxygen to tissues, with the associated oxygen–hemoglobin dissociation curve therefore shifted to the left. When methemoglobin concentration is elevated in red blood cells, tissue hypoxia can occur.
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 D74.0 and a single ICD9 code, 289.7 is an approximate match for comparison and conversion purposes.
Methemoglobin is a form of hemoglobin that contains ferric [Fe3+] iron and has a decreased ability to bind oxygen. However, the ferrous iron has an increased affinity for bound oxygen.
(Dorland, 27th ed) Codes. D74 Methemoglobinemia. D74.0 Congenital methem oglobinemia. D74.8 Other methemoglobinemias.
The presence of methemoglobin in the blood, resulting in cyanosis. A small amount of methemoglobin is present in the blood normally, but injury or toxic agents convert a larger proportion of hemoglobin into methemoglobin, which does not function reversibly as an oxygen carrier.
An inherited or acquired condition characterized by abnormally increased levels of methemoglobin in the blood. Signs and symptoms include cyanosis, dyspnea, headache, fatigue, mental status changes, and loss of consciousness. The presence of methemoglobin in the blood, resulting in cyanosis.
Symptoms may include headache, dizziness, fatigue, shortness of breath, nausea, vomiting, rapid heartbeat, loss of muscle coordination, and blue-colored skin. Methemoglobinemia can be caused by injury or being exposed to certain drugs, chemicals, or foods. It can also be an inherited condition.
Clinical Information. A condition in which a higher-than-normal amount of methemoglobin is found in the blood. Methemoglobin is a form of hemoglobin that cannot carry oxygen. In methemoglobinemia, tissues cannot get enough oxygen. Symptoms may include headache, dizziness, fatigue, shortness of breath, nausea, vomiting, rapid heartbeat, ...
The presence of methemoglobin in the blood, resulting in cyanosis. A small amount of methemoglobin is present in the blood normally, but injury or toxic agents convert a larger proportion of hemoglobin into methemoglobin, which does not function reversibly as an oxygen carrier.
neoplasms ( C00-D49) symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified ( R00 - R94) Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism. Clinical Information. A condition in which a higher-than-normal amount of methemoglobin is found in the blood.
Symptoms may include headache, dizziness, fatigue, shortness of breath, nausea, vomiting, rapid heartbeat, loss of muscle coordination, and blue-colored skin. Methemoglobinemia can be caused by injury or being exposed to certain drugs, chemicals, or foods. It can also be an inherited condition.
Methemoglobinemia may be due to a defect in the enzyme nadh methemoglobin reductase (an autosomal recessive trait) or to an abnormality in hemoglobin m (an autosomal dominant trait). (Dorland, 27th ed) Reimbursement claims with a date of service on or after October 1, 2015 require the use of ICD-10-CM codes.
An inherited or acquired condition characterized by abnormally increased levels of methemoglobin in the blood. Signs and symptoms include cyanosis, dyspnea, headache, fatigue, mental status changes, and loss of consciousness. The presence of methemoglobin in the blood, resulting in cyanosis.
Methemoglobinemia. Clinical Information. A condition in which a higher-than-normal amount of methemoglobin is found in the blood. Methemoglobin is a form of hemoglobin that cannot carry oxygen. In methemoglobinemia, tissues cannot get enough oxygen.
Symptoms may include headache, dizziness, fatigue, shortness of breath, nausea, vomiting, rapid heartbeat, loss of muscle coordination, and blue-colored skin. Methemoglobinemia can be caused by injury or being exposed to certain drugs, chemicals, or foods. It can also be an inherited condition.
A small amount of methemoglobin is present in the blood normally, but injury or toxic agents convert a larger proportion of hemoglobin into methemoglobin, which does not function reversibly as an oxygen carrier.
Methemoglobinemia (or methaemoglobinaemia) is a disorder characterized by the presence of a higher than normal level of methemoglobin (metHb, i.e., ferric [Fe3+] rather than ferrous [Fe2+] haemoglobin) in the blood. Methemoglobin is a form of hemoglobin that contains ferric [Fe3+] iron and has a decreased ability to bind oxygen.
The ICD-10-CM Alphabetical Index links the below-listed medical terms to the ICD code D74. Click on any term below to browse the alphabetical index.