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What is Brachymesophalangy 2 and 5?

What is Brachymesophalangy 2 and 5?

  • Brachymesophalangy 2 and 5: A rare genetic disorder characterized by short middle bones of the second and fifth fingers and toes.

Brachymesophalangy 2 and 5 is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Brachymesophalangy 2 and 5, or a subtype of Brachymesophalangy 2 and 5, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

Brachymesophalangy 2 and 5: Introduction

Types of Brachymesophalangy 2 and 5:

Broader types of Brachymesophalangy 2 and 5:

What causes Brachymesophalangy 2 and 5?

Causes of Brachymesophalangy 2 and 5: see causes of Brachymesophalangy 2 and 5

What are the symptoms of Brachymesophalangy 2 and 5?

Symptoms of Brachymesophalangy 2 and 5: see symptoms of Brachymesophalangy 2 and 5

Brachymesophalangy 2 and 5: Testing

Misdiagnosis: see misdiagnosis and Brachymesophalangy 2 and 5.

How is it treated?

Doctors and Medical Specialists for Brachymesophalangy 2 and 5: Medical Geneticist ; see also doctors and medical specialists for Brachymesophalangy 2 and 5.
Treatments for Brachymesophalangy 2 and 5: see treatments for Brachymesophalangy 2 and 5

Name and Aliases of Brachymesophalangy 2 and 5

Main name of condition: Brachymesophalangy 2 and 5

Other names or spellings for Brachymesophalangy 2 and 5:

temtamy type brachydactyly, Brachydactyly, type A4, BDA4, Brachydactyly Temtamy type

BDA4, Brachydactyly Temtamy type, Brachydactyly, type A4, Temtamy type brachydactyly
Source - Office of Rare Diseases (ORD) of the National Institutes of Health (NIH)

Brachymesophalangy 2 and 5: Related Conditions

Research the causes of these diseases that are similar to, or related to, Brachymesophalangy 2 and 5:

  • Rare inherited disorder
  • Short middle phalanges
 

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