icd 9 code for hypophosphatemia

What is the ICD 10 code for hypophosphatemia?

ICD-10-CM Diagnosis Code E83.39 [convert to ICD-9-CM] Other disorders of phosphorus metabolism Hyperphosphatemia; Hyperphosphatemia (high phosphate level); Hypophosphatasia; Hypophosphatemia; Hypophosphatemia (low phosphorus level); Rickets, hypophosphatasia; Acid phosphatase deficiency; Hypophosphatasia

What is the ICD 10 code for acid phosphatase deficiency?

Diagnosis Index entries containing back-references to E83.39: Acid phosphatase deficiency E83.39 Deficiency, deficient acid phosphatase E83.39 Diabetes, diabetic (mellitus) (sugar) E11.9 ICD-10-CM Diagnosis Code E11.9 Disorder (of) - see also Disease metabolism NOS E88.9 ICD-10-CM Diagnosis Code E88.9

What is the ICD 9 code for phosphorus metabolism?

Disorders of phosphorus metabolism Short description: Dis phosphorus metabol. ICD-9-CM 275.3 is a billable medical code that can be used to indicate a diagnosis on a reimbursement claim, however, 275.3 should only be used for claims with a date of service on or before September 30, 2015.

What are the symptoms of hypophosphatemia?

Hypophosphatemia is an electrolyte disorder in which there is a low level of phosphate in the blood. Symptoms may include weakness, trouble breathing, and loss of appetite.

What is the ICD 10 code for Hypophosphatemia?

E83. 31 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.

What ICD 10 covers phosphorus?

39.

What is phosphorus metabolism disorder?

Phosphorus metabolism disorders are the result of abnormal serum phosphate levels. These abnormal levels are caused by defects in the intake, excretion and cellular utilization of phosphate. Hypophosphataemia is a low blood level of phosphate, whereas hyperphosphataemia describes high levels of phosphate in the blood.

What is the ICD 10 code for hypomagnesemia?

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

What diagnosis covers phosphorus?

Disorder of phosphorus metabolism, unspecified E83. 30 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. 30 became effective on October 1, 2021.

What is the correct ICD-10 code for thrombocytopenia?

ICD-10 code D69. 6 for Thrombocytopenia, unspecified is a medical classification as listed by WHO under the range - Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism .

What is the most common cause of hypophosphatemia?

Hypophosphatemia is most often caused by long-term, relatively low phosphate intake in the setting of a sudden increase in intracellular phosphate requirements such as occurs with refeeding. Intestinal malabsorption can contribute to inadequate phosphate intake, especially if coupled with a poor diet.

Which of the following conditions is associated with hypophosphatemia?

Treatment. Hypophosphatemia affects the entire body, even on an intracellular level. If gone untreated, it can result in: Bone diseases like rickets, osteopenia, osteoporosis, and osteomalacia.

What is severe hypophosphatemia?

Severe chronic hypophosphatemia usually results from a prolonged negative phosphate balance. Causes include. Chronic starvation or malabsorption, often in patients with alcohol use disorder, especially when combined with vomiting or copious diarrhea.

What is the ICD-10 code for hyperphosphatemia?

39 - Other disorders of phosphorus metabolism is a sample topic from the ICD-10-CM. To view other topics, please log in or purchase a subscription. ICD-10-CM 2022 Coding Guide™ from Unbound Medicine.

What is the ICD-10 code for hypoglycemia?

ICD-10 code E16. 2 for Hypoglycemia, unspecified is a medical classification as listed by WHO under the range - Endocrine, nutritional and metabolic diseases .

What is the ICD-10 code for hypotension?

ICD-10 code I95. 9 for Hypotension, unspecified is a medical classification as listed by WHO under the range - Diseases of the circulatory system .

What is ICD-10 for hyperphosphatemia?

39 - Other disorders of phosphorus metabolism is a sample topic from the ICD-10-CM. To view other topics, please log in or purchase a subscription. ICD-10-CM 2022 Coding Guide™ from Unbound Medicine.

What is familial hypophosphatemia?

Familial hypophosphatemia is a term that describes a group of rare inherited disorders characterized by impaired kidney conservation of phosphate and in some cases, altered vitamin D metabolism.

What is hyperphosphatemia?

Hyperphosphatemia—that is, abnormally high serum phosphate levels—can result from increased phosphate intake, decreased phosphate excretion, or a disorder that shifts intracellular phosphate to extracellular space.

What can cause hyperphosphatemia?

Hyperphosphatemia is a serum phosphate concentration > 4.5 mg/dL (> 1.46 mmol/L). Causes include chronic kidney disease, hypoparathyroidism, and metabolic or respiratory acidosis. Clinical features may be due to accompanying hypocalcemia and include tetany.

How does hypophosphatemia occur?

Hypophosphatemia is caused by the following three mechanisms: 1 Inadequate intake (often unmasked in refeeding after long-term low phosphate intake) 2 Increased excretion (e.g. in hyperparathyroidism, hypophosphatemic rickets) 3 Shift of phosphorus from the extracellular to the intracellular space. This can be seen in treatment of diabetic ketoacidosis, refeeding, short-term increases in cellular demand (e.g. hungry bone syndrome) and acute respiratory alkalosis.

What causes a low phosphate level in the blood?

Causes include alcohol use disorder, refeeding in those with malnutrition, diabetic ketoacidosis, burns, hyperventilation, and certain medications. It may also occur in the setting of hyperparathyroidism, hypothyroidism, and Cushing syndrome. It is diagnosed based on a blood phosphate concentration of less than 0.81 mmol/L (2.5 mg/dL). When levels are below 0.32 mmol/L (1.0 mg/dL) it is deemed to be severe.

How to diagnose hypophosphatemia?

Hypophosphatemia is diagnosed by measuring the concentration of phosphate in the blood. Concentrations of phosphate less than 0.81 mmol/L (2.5 mg/dL) are considered diagnostic of hypophosphatemia, though additional tests may be needed to identify the underlying cause of the disorder.

How is phosphate given?

Phosphate may be given by mouth or by injection into a vein. Hypophosphatemia occurs in about 2% of people within hospital and 70% of people in the intensive care unit (ICU).

What is hypophosphatemia?

Hypophosphatemia is an electrolyte disorder in which there is a low level of phosphate in the blood. Symptoms may include weakness, trouble breathing, and loss of appetite. Complications may include seizures, coma, rhabdomyolysis, or softening of the bones.

Why does alkalemia occur?

This includes most common respiratory alkalemia (a higher than normal blood pH from low carbon dioxide levels in the blood), which in turn is caused by any hyperventilation (such as may result from sepsis, fever, pain, anxiety, drug withdrawal, and many other causes).

Why do cells need phosphate?

Causes. Refeeding syndrome – This causes a demand for phosphate in cells due to the action of hexokinase, an enzyme that attaches phosphate to glucose to begin metabolism of glucose. Also, production of ATP when cells are fed and recharge their energy supplies requires phosphate.

What is genetic metabolic disorder?

Genetic metabolic disorder resulting from serum and bone alkaline phosphatase deficiency leading to hypercalcemia, ethanolamine phosphatemia, and ethanolamine phosphaturia; manifestations include severe skeletal defects resembling vitamin d resistant rickets, failure of the calvarium to calcify, dyspnea, cyanosis, vomiting, constipation, renal calcinosis, failure to thrive, disorders of movement, beading of the costochondral junction, and rachitic bone changes.

What is a genetic disorder resulting from serum and bone alkaline phosphatase deficiency?

A genetic metabolic disorder resulting from serum and bone alkaline phosphatase deficiency leading to hypercalcemia, ethanolamine phosphatemia, and ethanolamine phosphaturia. Clinical manifestations include severe skeletal defects resembling vitamin d-resistant rickets, failure of the calvarium to calcify, dyspnea, cyanosis, vomiting, constipation, renal calcinosis, failure to thrive, disorders of movement, beading of the costochondral junction, and rachitic bone changes. (from Dorland, 27th ed)

What are the symptoms of a symtom?

The signs and symptoms vary significantly and include death in utero, failure to thrive, premature loss of deciduous teeth, early loss of the adult dentition, hypercalcemia, osteomalacia, skeletal defects, renal stones, and movement disorders.

When will the ICd 10 E83.39 be released?

The 2022 edition of ICD-10-CM E83.39 became effective on October 1, 2021.

Coding Notes for E83.39 Info for medical coders on how to properly use this ICD-10 code

Inclusion Terms are a list of concepts for which a specific code is used. The list of Inclusion Terms is useful for determining the correct code in some cases, but the list is not necessarily exhaustive.

ICD-10-CM Alphabetical Index References for 'E83.39 - Other disorders of phosphorus metabolism'

The ICD-10-CM Alphabetical Index links the below-listed medical terms to the ICD code E83.39. Click on any term below to browse the alphabetical index.

Equivalent ICD-9 Code GENERAL EQUIVALENCE MAPPINGS (GEM)

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 E83.39 and a single ICD9 code, 275.3 is an approximate match for comparison and conversion purposes.