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Rhizomelic chondrodysplasia punctata, type 1

Rhizomelic chondrodysplasia punctata, type 1: Introduction

Rhizomelic chondrodysplasia punctata, type 1: A rare genetic disorder involving abnormal development of bones which causes abnormal calcification of bones near the joints. The genetic defect is located on chromosome 6q22-q24. More detailed information about the symptoms, causes, and treatments of Rhizomelic chondrodysplasia punctata, type 1 is available below.

Symptoms of Rhizomelic chondrodysplasia punctata, type 1

Causes of Rhizomelic chondrodysplasia punctata, type 1

Read more about causes of Rhizomelic chondrodysplasia punctata, type 1.

Less Common Symptoms of Rhizomelic chondrodysplasia punctata, type 1

Statistics for Rhizomelic chondrodysplasia punctata, type 1

Rhizomelic chondrodysplasia punctata, type 1: Broader Related Topics

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Definitions of Rhizomelic chondrodysplasia punctata, type 1:

Rhizomelic chondrodysplasia punctata, 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 Rhizomelic chondrodysplasia punctata, type 1, or a subtype of Rhizomelic chondrodysplasia punctata, type 1, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

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More information about Rhizomelic chondrodysplasia punctata, type 1

  1. Rhizomelic chondrodysplasia punctata, type 1: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
 

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