2024 ICD-10-CM Diagnosis Code E87.2
Specific Coding Applicable to Acidosis
Non-specific codes like E87.2 require more digits to indicate the appropriate level of specificity. Consider using any of the following ICD-10-CM codes with a higher level of specificity when coding for acidosis:
Clinical Category is Fluid and electrolyte disorders
- CCSR Category Code: END011
- Inpatient Default CCSR: Y - Yes, default inpatient assignment for principal diagnosis or first-listed diagnosis.
- Outpatient Default CCSR: Y - Yes, default outpatient assignment for principal diagnosis or first-listed diagnosis.
Acidosisa pathologic condition of acid accumulation or depletion of base in the body. the two main types are respiratory acidosis and metabolic acidosis, due to metabolic acid build up.
Acidosis, Lacticacidosis caused by accumulation of lactic acid more rapidly than it can be metabolized. it may occur spontaneously or in association with diseases such as diabetes mellitus; leukemia; or liver failure.
Acidosis, Renal Tubulara group of genetic disorders of the kidney tubules characterized by the accumulation of metabolically produced acids with elevated plasma chloride, hyperchloremic metabolic acidosis. defective renal acidification of urine (proximal tubules) or low renal acid excretion (distal tubules) can lead to complications such as hypokalemia, hypercalcinuria with nephrolithiasis and nephrocalcinosis, and rickets.
Acidosis, Respiratoryrespiratory retention of carbon dioxide. it may be chronic or acute.
Diabetic Ketoacidosisa life-threatening complication of diabetes mellitus, primarily of type 1 diabetes mellitus with severe insulin deficiency and extreme hyperglycemia. it is characterized by ketosis; dehydration; and depressed consciousness leading to coma.
Hypoaldosteronisma congenital or acquired condition of insufficient production of aldosterone by the adrenal cortex leading to diminished aldosterone-mediated synthesis of na(+)-k(+)-exchanging atpase in renal tubular cells. clinical symptoms include hyperkalemia, sodium-wasting, hypotension, and sometimes metabolic acidosis.
Acidosisan abnormally high acidity of the blood and other body tissues. acidosis can be either respiratory or metabolic.
Acidosisan abnormally high acidity (excess hydrogen-ion concentration) of the blood and other body tissues.
Acidosis, CTCAE|Acidosis|Acidosisa disorder characterized by abnormally high acidity (high hydrogen-ion concentration) of the blood and other body tissues.
Autosomal Recessive Distal Renal Tubular Acidosis-4 with Hemolytic Anemia|DRTA4an autosomal recessive type of distal renal tubular acidosis caused by mutation(s) in the slc4a1 gene, encoding band 3 anion transport protein. additionally, it may be characterized by hemolytic anemia.
Diabetes Mellitus due to Underlying Condition with Ketoacidosis with Coma|Diabetes mellitus due to underlying condition with ketoacidosis with comaevidence of diabetes mellitus due to underlying condition with ketoacidosis with coma.
Diabetes Mellitus due to Underlying Condition with Ketoacidosis without Coma|Diabetes mellitus due to underlying condition with ketoacidosis without comaevidence of diabetes mellitus due to underlying condition with ketoacidosis without coma.
Diabetic Ketoacidosis|DKA|DKA|Elevated Ketones/Diabetic Ketoacidosisthe metabolic condition resulted from uncontrolled diabetes mellitus, in which the shift of acid-base status of the body toward the acid side because of loss of base or retention of acids other than carbonic acid is accompanied by the accumulation of ketone bodies in body tissues and fluids.
Distal Renal Tubular Acidosisfailure of the renal tubules of the kidney to excrete urine of sufficient acidity, resulting in metabolic acidosis.
Drug or Chemical Induced Diabetes Mellitus with Ketoacidosis with Coma|Drug or chemical induced diabetes mellitus with ketoacidosis with comaevidence of drug or chemical induced diabetes mellitus with ketoacidosis with coma.
Drug or Chemical Induced Diabetes Mellitus with Ketoacidosis without Coma|Drug or chemical induced diabetes mellitus with ketoacidosis without comaevidence of drug or chemical induced diabetes mellitus with ketoacidosis without coma.
Fetal Acidosis|Fetal Acidemia|Fetal Acidemiaan abnormally high hydrogen ion concentration (umbilical arterial blood ph less than 7.00) in fetal blood or tissue.
Grade 1 Acidosis, CTCAE|Grade 1 Acidosisph
Grade 3 Acidosis, CTCAE|Grade 3 Acidosisph <7.3
Grade 4 Acidosis, CTCAE|Grade 4 Acidosislife-threatening consequences
Grade 5 Acidosis, CTCAE|Grade 5 Acidosisdeath
Lactic Acidosismetabolic acidosis characterized by the accumulation of lactate in the body. it is caused by tissue hypoxia.
MELAS Syndrome|MELAS|Mitochondrial Encephalomyopathy, Lactic Acidosis and Strokea rare progressive neurodegenerative disorder characterized by mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes.
Metabolic Acidosis|Acidosis|metabolic acidosisincreased acidity in the blood secondary to acid base imbalance. causes include diabetes, kidney failure and shock.
Osteopetrosis with Renal Tubular Acidosis|Autosomal Recessive Osteopetrosis 3|Autosomal Recessive Osteopetrosis, Type 3|Carbonic Anhydrase II Deficiency|Guibaud-Vainsel Syndrome|Marble Brain Disease|OPTB3a rare, autosomal recessive inherited disorder caused by mutation in the ca2 gene. it is characterized by osteopetrosis, renal tubular acidosis, and cerebral calcifications. it results in growth failure, mental retardation, and fractures.
Other Specified Diabetes Mellitus with Ketoacidosis with Coma|Other specified diabetes mellitus with ketoacidosis with comaevidence of other specified diabetes mellitus with ketoacidosis with coma not specified elsewhere.
Other Specified Diabetes Mellitus with Ketoacidosis without Coma|Other specified diabetes mellitus with ketoacidosis without comaevidence of other specified diabetes mellitus with ketoacidosis without coma not specified elsewhere.
Proximal Renal Tubular Acidosis|Type II Renal Tubular Acidosisimpairment in renal proximal tubule bicarbonate reabsorption that results in a hypokalemic hyperchloremic metabolic acidosis, which is most commonly associated with renal fanconi syndrome.
Renal Tubular Acidosis Associated With Deafnessrenal tubular acidosis associated with sensorineural hearing loss, and which is typically associated with recessive mutations.
Renal Tubular Acidosis|renal tubular acidosisthe inability of the kidneys to maintain acid-base homeostasis.
Respiratory Acidosisacid base imbalance resulting from an accumulation of carbon dioxide secondary to hypoventilation.
Respiratory Acidosis|Hypercapnic Acidosisa condition in which the blood ph is less than normal, secondary to impaired gas exchange.
Type 1 Diabetes Mellitus with Ketoacidosis with Coma|Type 1 diabetes mellitus with ketoacidosis with comaevidence of type 1 diabetes mellitus with ketoacidosis with coma.
Type 1 Diabetes Mellitus with Ketoacidosis without Coma|Type 1 diabetes mellitus with ketoacidosis without comaevidence of type 1 diabetes mellitus with ketoacidosis without coma.
Type 2 Diabetes Mellitus with Ketoacidosis with Coma|Type 2 diabetes mellitus with ketoacidosis with comaevidence of type 2 diabetes mellitus with ketoacidosis with coma.
Type 2 Diabetes Mellitus with Ketoacidosis without Coma|Type 2 diabetes mellitus with ketoacidosis without comaevidence of type 2 diabetes mellitus with ketoacidosis without coma.
Type I Renal Tubular Acidosisimpairment in renal collecting tubule acid secretion that results in a hypokalemic hyperchloremic metabolic acidosis.
Tabular List of Diseases and Injuries
The following annotation back-references are applicable to this diagnosis code. The Tabular List of Diseases and Injuries is a list of ICD-10-CM codes, organized "head to toe" into chapters and sections with coding notes and guidance for inclusions, exclusions, descriptions and more.
Type 1 ExcludesType 1 Excludes
A type 1 excludes note is a pure excludes note. It means "NOT CODED HERE!" An Excludes1 note indicates that the code excluded should never be used at the same time as the code above the Excludes1 note. An Excludes1 is used when two conditions cannot occur together, such as a congenital form versus an acquired form of the same condition.
Metabolism is the process your body uses to get or make energy from the food you eat. Food is made up of proteins, carbohydrates, and fats. Chemicals in your digestive system break the food parts down into sugars and acids, your body's fuel. Your body can use this fuel right away, or it can store the energy in your body tissues, such as your liver, muscles, and body fat.
A metabolic disorder occurs when abnormal chemical reactions in your body disrupt this process. When this happens, you might have too much of some substances or too little of other ones that you need to stay healthy. There are different groups of disorders. Some affect the breakdown of amino acids, carbohydrates, or lipids. Another group, mitochondrial diseases, affects the parts of the cells that produce the energy.
You can develop a metabolic disorder when some organs, such as your liver or pancreas, become diseased or do not function normally. Diabetes is an example.
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- FY 2024 - No Change, effective from 10/1/2023 through 9/30/2024
- FY 2023 - Code Added, effective from 10/1/2022 through 9/30/2023
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- FY 2016 - New Code, effective from 10/1/2015 through 9/30/2016. This was the first year ICD-10-CM was implemented into the HIPAA code set.
 Not chronic - A diagnosis code that does not fit the criteria for chronic condition (duration, ongoing medical treatment, and limitations) is considered not chronic. Some codes designated as not chronic are acute conditions. Other diagnosis codes that indicate a possible chronic condition, but for which the duration of the illness is not specified in the code description (i.e., we do not know the condition has lasted 12 months or longer) also are considered not chronic.