Rdcrn Portal

Access your rdcrn portal account from the list of rdcrn portal pages listed below.

Find Diseases By Category | Genetic And Rare Diseases ...

RDCRN; Skin Diseases; Viral infections; List of FDA Orphan Drugs. GARD Information Navigator. FAQs About Rare Diseases. Find Diseases By Category Diseases are grouped into categories to help you find related conditions. Many of the categories cover a specific body system. The classifications mostly come from Orphanet, a European portal for rare disease information. …

Síndrome De Williams | Genetic And Rare Diseases ...

El síndrome de Williams es una enfermedad genética que afecta muchas partes del cuerpo. Se caracteriza por discapacidad intelectual leve a moderada, personalidad con características únicas, rostro distintivo, problemas del corazón, y vasos sanguíneos (cardiovascular). El síndrome de Williams es causado por falta de algunos genes de una región específica del cromosoma 7.

National COVID Cohort Collaborative (N3C) | National ...

2021-12-06  · The N3C is a partnership among the NCATS-supported Clinical and Translational Science Awards (CTSA) Program hubs, the National Center for Data to Health (CD2H), and NIGMS-supported Institutional Development Award Networks for Clinical and Translational Research (IDeA-CTR), with overall stewardship by NCATS.Collaborators will contribute and use …

About NCATS | National Center For Advancing Translational ...

2021-04-16  · The National Center for Advancing Translational Sciences (NCATS) — one of 27 Institutes and Centers at the National Institutes of Health (NIH) — was established to transform the translational process so that new treatments and cures for disease can be delivered to patients faster. Learn more.

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