ICD-10-CM Code E26.81

Bartter's syndrome

Version 2021 Billable Code

Valid for Submission

E26.81 is a billable code used to specify a medical diagnosis of bartter's syndrome. The code is valid for the fiscal year 2021 for the submission of HIPAA-covered transactions. The ICD-10-CM code E26.81 might also be used to specify conditions or terms like bartter syndrome, bartter syndrome antenatal type 1, bartter syndrome antenatal type 2, bartter syndrome type 3, bartter syndrome type 4, bartter syndrome type 4a, etc

ICD-10:E26.81
Short Description:Bartter's syndrome
Long Description:Bartter's syndrome

Index to Diseases and Injuries

The Index to Diseases and Injuries is an alphabetical listing of medical terms, with each term mapped to one or more ICD-10 code(s). The following references for the code E26.81 are found in the index:


Synonyms

The following clinical terms are approximate synonyms or lay terms that might be used to identify the correct diagnosis code:

  • Bartter syndrome
  • Bartter syndrome antenatal type 1
  • Bartter syndrome antenatal type 2
  • Bartter syndrome type 3
  • Bartter syndrome type 4
  • Bartter syndrome type 4a
  • Disorder of fetal abdominal region
  • Disorder of fetal abdominal region
  • Hypochloremic alkalosis

Clinical Information

  • BARTTER SYNDROME-. a group of disorders caused by defective salt reabsorption in the ascending loop of henle. it is characterized by severe salt wasting hypokalemia; hypercalciuria; metabolic alkalosis and hyper reninemic hyperaldosteronism without hypertension. there are several subtypes including ones due to mutations in the renal specific sodium potassium chloride symporters.

Diagnostic Related Groups

The ICD-10 code E26.81 is grouped in the following groups for version MS-DRG V38.0 What are Diagnostic Related Groups?
The Diagnostic Related Groups (DRGs) are a patient classification scheme which provides a means of relating the type of patients a hospital treats. The DRGs divides all possible principal diagnoses into mutually exclusive principal diagnosis areas referred to as Major Diagnostic Categories (MDC).
applicable from 10/01/2020 through 09/30/2021.

  • 643 - ENDOCRINE DISORDERS WITH MCC
  • 644 - ENDOCRINE DISORDERS WITH CC
  • 645 - ENDOCRINE DISORDERS WITHOUT CC/MCC

Convert E26.81 to ICD-9

Code Classification

  • Endocrine, nutritional and metabolic diseases (E00–E90)
    • Disorders of other endocrine glands (E20-E35)
      • Hyperaldosteronism (E26)

Code History

  • FY 2016 - New Code, effective from 10/1/2015 through 9/30/2016
    (First year ICD-10-CM implemented into the HIPAA code set)
  • FY 2017 - No Change, effective from 10/1/2016 through 9/30/2017
  • FY 2018 - No Change, effective from 10/1/2017 through 9/30/2018
  • FY 2019 - No Change, effective from 10/1/2018 through 9/30/2019
  • FY 2020 - No Change, effective from 10/1/2019 through 9/30/2020
  • FY 2021 - No Change, effective from 10/1/2020 through 9/30/2021

Information for Patients


Adrenal Gland Disorders

The adrenal glands are small glands located on top of each kidney. They produce hormones that you can't live without, including sex hormones and cortisol. Cortisol helps you respond to stress and has many other important functions.

With adrenal gland disorders, your glands make too much or not enough hormones. In Cushing's syndrome, there's too much cortisol, while with Addison's disease, there is too little. Some people are born unable to make enough cortisol.

Causes of adrenal gland disorders include

  • Genetic mutations
  • Tumors including pheochromocytomas
  • Infections
  • A problem in another gland, such as the pituitary, which helps to regulate the adrenal gland
  • Certain medicines

Treatment depends on which problem you have. Surgery or medicines can treat many adrenal gland disorders.

NIH: National Institute of Child Health and Human Development

  • 17-hydroxycorticosteroids (Medical Encyclopedia)
  • 17-OH progesterone (Medical Encyclopedia)
  • 24-hour urinary aldosterone excretion rate (Medical Encyclopedia)
  • ACTH (cosyntropin) stimulation test (Medical Encyclopedia)
  • ACTH blood test (Medical Encyclopedia)
  • Acute adrenal crisis (Medical Encyclopedia)
  • Adrenal glands (Medical Encyclopedia)
  • Adrenalectomy (Medical Encyclopedia)
  • Aldosterone blood test (Medical Encyclopedia)
  • Congenital adrenal hyperplasia (Medical Encyclopedia)
  • Hyperaldosteronism - primary and secondary (Medical Encyclopedia)

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Kidney Diseases

Also called: Renal disease

You have two kidneys, each about the size of your fist. They are near the middle of your back, just below the rib cage. Inside each kidney there are about a million tiny structures called nephrons. They filter your blood. They remove wastes and extra water, which become urine. The urine flows through tubes called ureters. It goes to your bladder, which stores the urine until you go to the bathroom.

Most kidney diseases attack the nephrons. This damage may leave kidneys unable to remove wastes. Causes can include genetic problems, injuries, or medicines. You have a higher risk of kidney disease if you have diabetes, high blood pressure, or a close family member with kidney disease. Chronic kidney disease damages the nephrons slowly over several years. Other kidney problems include

  • Cancer
  • Cysts
  • Stones
  • Infections

Your doctor can do blood and urine tests to check if you have kidney disease. If your kidneys fail, you will need dialysis or a kidney transplant.

NIH: National Institute of Diabetes and Digestive and Kidney Diseases

  • ACE inhibitors (Medical Encyclopedia)
  • Acute nephritic syndrome (Medical Encyclopedia)
  • Analgesic nephropathy (Medical Encyclopedia)
  • Atheroembolic renal disease (Medical Encyclopedia)
  • Bartter syndrome (Medical Encyclopedia)
  • Bilateral hydronephrosis (Medical Encyclopedia)
  • Congenital nephrotic syndrome (Medical Encyclopedia)
  • Distal renal tubular acidosis (Medical Encyclopedia)
  • Focal segmental glomerulosclerosis (Medical Encyclopedia)
  • Glomerulonephritis (Medical Encyclopedia)
  • Goodpasture syndrome (Medical Encyclopedia)
  • IgA nephropathy (Medical Encyclopedia)
  • Injury - kidney and ureter (Medical Encyclopedia)
  • Interstitial nephritis (Medical Encyclopedia)
  • Kidney removal (Medical Encyclopedia)
  • Kidney removal - discharge (Medical Encyclopedia)
  • Membranoproliferative GN I (Medical Encyclopedia)
  • Membranous nephropathy (Medical Encyclopedia)
  • Minimal change disease (Medical Encyclopedia)
  • Nephrocalcinosis (Medical Encyclopedia)
  • Nephrotic syndrome (Medical Encyclopedia)
  • Obstructive uropathy (Medical Encyclopedia)
  • Perirenal abscess (Medical Encyclopedia)
  • Proximal renal tubular acidosis (Medical Encyclopedia)
  • Reflux nephropathy (Medical Encyclopedia)
  • Renal papillary necrosis (Medical Encyclopedia)
  • Renal vein thrombosis (Medical Encyclopedia)
  • Unilateral hydronephrosis (Medical Encyclopedia)

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Bartter syndrome Bartter syndrome is a group of very similar kidney disorders that cause an imbalance of potassium, sodium, chloride, and related molecules in the body.In some cases, Bartter syndrome becomes apparent before birth. The disorder can cause polyhydramnios, which is an increased volume of fluid surrounding the fetus (amniotic fluid). Polyhydramnios increases the risk of premature birth.Beginning in infancy, affected individuals often fail to grow and gain weight at the expected rate (failure to thrive). They lose excess amounts of salt (sodium chloride) in their urine, which leads to dehydration, constipation, and increased urine production (polyuria). In addition, large amounts of calcium are lost through the urine (hypercalciuria), which can cause weakening of the bones (osteopenia). Some of the calcium is deposited in the kidneys as they are concentrating urine, leading to hardening of the kidney tissue (nephrocalcinosis). Bartter syndrome is also characterized by low levels of potassium in the blood (hypokalemia), which can result in muscle weakness, cramping, and fatigue. Rarely, affected children develop hearing loss caused by abnormalities in the inner ear (sensorineural deafness).Two major forms of Bartter syndrome are distinguished by their age of onset and severity. One form begins before birth (antenatal) and is often life-threatening. The other form, often called the classical form, begins in early childhood and tends to be less severe. Once the genetic causes of Bartter syndrome were identified, researchers also split the disorder into different types based on the genes involved. Types I, II, and IV have the features of antenatal Bartter syndrome. Because type IV is also associated with hearing loss, it is sometimes called antenatal Bartter syndrome with sensorineural deafness. Type III usually has the features of classical Bartter syndrome.
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