Course:MEDG550/Student Activities
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Past Student Activities
- Barth Syndrome
- CHARGE Syndrome
- Non-Syndromic Retinitis Pigmentosa
- Stargardt Disease
- Gorlin Syndrome
- Krabbe Disease
- Pompe Disease
- Pfeiffer Syndrome
- Hypophosphatasia
- Menkes Disease
- Fibrodysplasia Ossificans Progressiva (Stoneman Disease, or Münchmeyer Disease)
- Galloway-Mowat Syndrome
- Prader-Willi Syndrome
- Friedreich's ataxia
- Apert Syndrome
- Mitochondrial DNA Depletion Syndrome
- DICER-1 Syndrome
- Machado-Joseph Disease
- Dilated Cardiomyopathy
- Hemochromatosis
- Noonan Syndrome
- Alport Syndrome
- Polycystic Kidney Disease (PKD)
- Fragile-X Syndrome
- Duchenne and Becker Muscular Dystrophy
- Wolf Hirschhorn Syndrome
- Long QT Syndrome
- Williams Syndrome
- Cri-du-chat Syndrome
- Zellweger Spectrum Disorder
- DiGeorge Syndrome
- Kabuki Syndrome
- Achondroplasia
- Smith-Magenis Syndrome
- Waardenburg Syndrome Type I
- Huntington's Disease
- Vascular Ehlers-Danlos Syndrome (vEDS)
- Spinal Muscular Atrophy
- Wilson Disease
- Neurofibromatosis
- Hemophilia A
- Tay-Sachs
- Angelman Syndrome
- Cystic Fibrosis
- Fabry Disease
- Factor V Leiden Thrombophilia
- Phenylketonuria (PKU)
- Werner Syndrome
- Glucose 6-Phosphate Dehydrogenase Deficiency
- Loeys-Dietz syndrome (LDS)
- Gaucher Disease
- Klinefelter Syndrome
- Familial Mediterranean Fever
- Osteogenesis Imperfecta
- Marfan Syndrome
- Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC)
- Dystrophic Epidermolysis Bullosa
- Primary Ciliary Dyskinesia
- Turner's Syndrome
- Myotonic Dystrophy
- Alpha-1 Antitrypsin Deficiency
- Sickle Cell Disease
- Hypertrophic Cardiomyopathy (HCM)
- Canavan Disease
- Charcot-Marie-Tooth Disease, Type 1
- Beckwith-Wiedemann Syndrome
- Treacher Collins Syndrome
- Rett Syndrome
- Familial Hemiplegic Migraine
- Carnitine Uptake Deficiency
- Li-Fraumeni Syndrome
- Primary Hyperoxaluria Type 1
- Brugada Syndrome
- Hereditary Hemorrhagic Telangiectasia (HHT)
- Usher Syndrome
- Beta-Thalassemia
- Myotubular Myopathy
- Malignant Hyperthermia Susceptibility (MHS)
- Urbach-Wiethe Disease
- X-linked Retinoschisis