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Faciodigitogenital syndrome, recessive form

Faciodigitogenital syndrome, recessive form: Introduction

Faciodigitogenital syndrome, recessive form: A rare syndrome characterized by facial, digital and genital abnormalities. More detailed information about the symptoms, causes, and treatments of Faciodigitogenital syndrome, recessive form is available below.

Symptoms of Faciodigitogenital syndrome, recessive form

Home Diagnostic Testing

Home medical testing related to Faciodigitogenital syndrome, recessive form:

Wrongly Diagnosed with Faciodigitogenital syndrome, recessive form?

Faciodigitogenital syndrome, recessive form: Related Patient Stories

Causes of Faciodigitogenital syndrome, recessive form

Read more about causes of Faciodigitogenital syndrome, recessive form.

Faciodigitogenital syndrome, recessive form: Undiagnosed Conditions

Commonly undiagnosed diseases in related medical categories:

Misdiagnosis and Faciodigitogenital syndrome, recessive form

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Hair and scalp disorders misdiagnosed in African Americans: A higher than average percentage of misdiagnoses of hair or scalp disorders seem to occur in African Americans. Some of the overlooked hair/scalp conditions include...read more »

Faciodigitogenital syndrome, recessive form: Research Doctors & Specialists

Research related physicians and medical specialists:

Other doctor, physician and specialist research services:

Hospitals & Clinics: Faciodigitogenital syndrome, recessive form

Research quality ratings and patient safety measures for medical facilities in specialties related to Faciodigitogenital syndrome, recessive form:

Choosing the Best Hospital: More general information, not necessarily in relation to Faciodigitogenital syndrome, recessive form, on hospital performance and surgical care quality:

Faciodigitogenital syndrome, recessive form: Animations

Statistics for Faciodigitogenital syndrome, recessive form

Faciodigitogenital syndrome, recessive form: Broader Related Topics

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Definitions of Faciodigitogenital syndrome, recessive form:

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

 

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