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Hypocalciuric hypercalcemia, familial, type 1

Hypocalciuric hypercalcemia, familial, type 1: Introduction

Hypocalciuric hypercalcemia, familial, type 1: Familial hypocalciuric hypercalcemia is an inherited benign disorder of calcium metabolism which results in high blood calcium levels and low urine calcium levels. The condition is generally asymptomatic and the abnormality is discovered incidentally during blood tests. Subtype 2 involves a genetic defect on chromosome 3q13.3-q21. More detailed information about the symptoms, causes, and treatments of Hypocalciuric hypercalcemia, familial, type 1 is available below.

Symptoms of Hypocalciuric hypercalcemia, familial, type 1

Home Diagnostic Testing

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Causes of Hypocalciuric hypercalcemia, familial, type 1

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Misdiagnosis and Hypocalciuric hypercalcemia, familial, type 1

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Hypocalciuric hypercalcemia, familial, type 1: Research Doctors & Specialists

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Hypocalciuric hypercalcemia, familial, type 1: Animations

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Definitions of Hypocalciuric hypercalcemia, familial, type 1:

Hypocalciuric hypercalcemia, familial, type 1 is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Hypocalciuric hypercalcemia, familial, type 1, or a subtype of Hypocalciuric hypercalcemia, familial, type 1, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

Related Hypocalciuric hypercalcemia, familial, type 1 Info

More information about Hypocalciuric hypercalcemia, familial, type 1

  1. Hypocalciuric hypercalcemia, familial, type 1: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
  6. Home Testing
 

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