Mystery Diagnosis of Rare Diseases
Rare diseases affect an estimated 2-4% of the population. A likely next step is whole genome sequencing, a diagnostic technique that over the last decade has significantly bolstered the effort to identify undiscovered diseases. A different approach is to search for patients with similar hereditary abnormalities and similar side effects. Determining the cause of a malady is often a victory in its own right for people who’ve spent years trying to figure out what’s wrong with their bodies.
Related Conference of Mystery Diagnosis of Rare Diseases
December 11-12, 2025
6th International Conference on Breast Pathology and Cancer Diagnosis
Amsterdam, Netherlands
Mystery Diagnosis of Rare Diseases Conference Speakers
Recommended Sessions
- Allergic and Immunologic Disorders
- Challenges of Living with Rare Diseases
- Clinical Research and Treatment
- Future of Rare Diseases Research
- Gene Therapy for Rare Diseases
- Infectious Diseases
- Mystery Diagnosis of Rare Diseases
- Neglected Tropical Diseases
- Orphan diseases and public health
- Orphan Drug
- Rare Autoimmune Diseases
- Rare Diseases
- Rare Endocrine Genetic Diseases
- Rare Genetic Diseases
- Rare Hematology Diseases
- Rare Neurological Disorders
- Rare Obesity and Metabolic Disorders
- Rare Pediatrics Diseases
- Rare Skin Diseases
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