icd 10 code for hypomagnesmia

by Dr. Kayden Satterfield I 4 min read

ICD-10 code E83. 42 for Hypomagnesemia is a medical classification as listed by WHO under the range - Endocrine, nutritional and metabolic diseases .

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What is the DX code for magnesium?

Group 1CodeDescription83735MAGNESIUM

What is the ICD-10 code for Hypermagnesemia?

ICD-10-CM Code for Hypermagnesemia E83. 41.

What is the ICD-10 code for hypotension?

ICD-10 code I95 for Hypotension is a medical classification as listed by WHO under the range - Diseases of the circulatory system .

What is the ICD-10 code for generalized weakness?

ICD-10 code M62. 81 for Muscle weakness (generalized) is a medical classification as listed by WHO under the range - Soft tissue disorders .

What causes hypomagnesemia?

Hypomagnesemia is an electrolyte disturbance caused when there is a low level of serum magnesium (less than 1.46 mg/dL) in the blood. Hypomagnesemia can be attributed to chronic disease, alcohol use disorder, gastrointestinal losses, renal losses, and other conditions.

What is the ICD-10 code for hyperglycemia?

ICD-10-CM Code for Hyperglycemia, unspecified R73. 9.

What is the ICD-10 code for bradycardia?

ICD-10 code: R00. 1 Bradycardia, unspecified | gesund.bund.de.

Can you have hypotension and hypertension at the same time?

The incidence of both orthostatic hypotension (OH) and hypertension increases with age, arguably in relation to a decrease in autonomic and baroreflex function. It is not surprising, therefore, that they often coexist.

What is the ICD-10 for hypertension?

ICD-10 uses only a single code for individuals who meet criteria for hypertension and do not have comorbid heart or kidney disease. That code is I10, Essential (primary) hypertension.

What is the ICD 10 code for weakness and fatigue?

ICD-10-CM Code for Other malaise and fatigue R53. 8.

What is the ICD 10 code for lower extremity weakness?

R53. 1 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 R53. 1 became effective on October 1, 2021.

How do you code left weaknesses in ICD-10?

Hemiplegia, unspecified affecting left dominant side The 2022 edition of ICD-10-CM G81. 92 became effective on October 1, 2021.

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 E83.42 are found in the index:

Approximate Synonyms

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

Clinical Information

GITELMAN SYNDROME-. an inherited renal disorder characterized by defective nacl reabsorption in the convoluted distal kidney tubule leading to hypokalemia.

Convert E83.42 to ICD-9 Code

The General Equivalency Mapping (GEM) crosswalk indicates an approximate mapping between the ICD-10 code E83.42 its ICD-9 equivalent. The approximate mapping means there is not an exact match between the ICD-10 code and the ICD-9 code and the mapped code is not a precise representation of the original code.

Information for Patients

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.

What is the ICd code for hypomagnesemia?

E83.42 is a billable ICD code used to specify a diagnosis of hypomagnesemia. A 'billable code' is detailed enough to be used to specify a medical diagnosis.

What is the approximate match between ICd9 and ICd10?

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 E83.42 and a single ICD9 code, 275.2 is an approximate match for comparison and conversion purposes.

What is Gitelman syndrome?

Gitelman syndrome is an autosomal recessive kidney disorder characterized by hypokalemic metabolic alkalosis with hypocalciuria, and hypomagnesemia. It is caused by loss of function mutations of the thiazide sensitive sodium-chloride symporter (also known as NCC, NCCT, or TSC) located in the distal convoluted tubule.

What is DRG #640-641?

DRG Group #640-641 - Misc disorders of nutrition, metabolism, fluids or electrolytes with MCC.

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