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Finding useful health information on the Internet can be difficult, but we’re here to help. This page gathers quality information from trusted sources. You can learn more about the disease, visit handpicked websites, and find resources to help you in your daily life. Need more information? Click the menu on the left to find more!

 

Syndactyly

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Overview

Type of Disease: Chromosomal Genetic, autosomal recessive Genetic, autosomal dominant Genetic, X-linked Congenital onset

Trusted Medical Sites

Genetic & Rare Diseases Information Center (GARD) GARD provides the public with access to current, reliable, and easy-to-understand information about rare or genetic diseases in English or Spanish.

Support Organizations

Support organizations can provide help and guidance in areas such as peer matching, education and training, and therapy and counseling.

Disease Resources

Resources can help guide your quest for factual and reliable information.
Displaying 1-5 of 6 results.
AAMDSIF Online Academy (webinars)
Added On: Dec 18, 2018
Category: General
200+ FREE webinars for patients, families and caregivers about rare blood cancers and bone marrow failure diseases.
Educational Resources
Added On: Dec 18, 2018
Category: General
Publications, links to patient conferences and webinars
Disease Information
Added On: Dec 18, 2018
Category: General
Descriptions of various rare blood cancers and bone marrow failure diseases.
Research Grants
Added On: Jul 7, 2015
Category: General
NFS provides research grants as funds are available. Grants are submitted by July annually and if approved, are awarded each September. Grant are only available for qualified research initiatives and are not available for administrative support.
Family Support
Added On: Jul 7, 2015
Category: General
NFS serves as a resource to families afflicted by Syndactyly or any related congenial hand or feet birth defects.