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Tibial aplasia ectrodactyly

Tibial aplasia ectrodactyly: Introduction

Tibial aplasia ectrodactyly: A rare genetic disorder characterized by split hands and/or feet and absence of long bones of the arms or legs. More detailed information about the symptoms, causes, and treatments of Tibial aplasia ectrodactyly is available below.

Symptoms of Tibial aplasia ectrodactyly

Wrongly Diagnosed with Tibial aplasia ectrodactyly?

Tibial aplasia ectrodactyly: Related Patient Stories

Tibial aplasia ectrodactyly: Deaths

Read more about Deaths and Tibial aplasia ectrodactyly.

Causes of Tibial aplasia ectrodactyly

Read more about causes of Tibial aplasia ectrodactyly.

More information about causes of Tibial aplasia ectrodactyly:

Disease Topics Related To Tibial aplasia ectrodactyly

Research the causes of these diseases that are similar to, or related to, Tibial aplasia ectrodactyly:

Less Common Symptoms of Tibial aplasia ectrodactyly

Misdiagnosis and Tibial aplasia ectrodactyly

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Tibial aplasia ectrodactyly: Research Doctors & Specialists

Research related physicians and medical specialists:

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Tibial aplasia ectrodactyly: Animations

Statistics for Tibial aplasia ectrodactyly

Tibial aplasia ectrodactyly: Broader Related Topics

User Interactive Forums

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Definitions of Tibial aplasia ectrodactyly:

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

Ophanet, a consortium of European partners, currently defines a condition rare when it affects 1 person per 2,000. They list Tibial aplasia ectrodactyly as a "rare disease".
Source - Orphanet


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