Fabry Support & Information Group (Fabry Disease)

Facioscapulohumeral Muscular Dystrophy Society (FSH Society) ( Facio-Scapulo-Humeral Muscular Dystrophy, Muscular Dystrophy)

Familial Exudative Vitreoretinopathy (fevr.net) (Familial Exudative Vitreoretinopathy)

Familial Gastrointestinal Cancer Registry (FAP- Familial Adenomatous Polyposis, Gastrointestinal Cancer)

Families of Spinal Muscular Atrophy Canada (Spinal Muscular Atrophy-SMA, Infantile Progressive Spinal Muscular Atrophy, Werdnig-Hoffman Disease, Juvenile Progressive Muscular Atrophy, Kugelberg-Welander Disease, Adult Progressive Spinal Muscualr Atrophy, Aran-Duchenne Type)

Fanconi Canada (Fanconi Anemia)

Fatty Oxidation Disorders(FOD) Family Support Group (Fatty Oxidation Disorders: Carnitine Transport Defect (Primary Carnitine Deficiency), Carnitine-Acylcarnitine Translocase Deficiency (Translocase), Carnitine Palmitoyl Transferase I & II (CPT I & II) Deficiency, Very Long Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency, Long Chain 3-Hydroxyacyl-CoA Dehydrogenase (LCHAD) Deficiency, Trifunctional Protein (TFP) Deficiency, Medium Chain Acyl-CoA Dehydrogenase (MCAD) Deficiency, 2,4 Dienoyl-CoA Reductase Deficiency, Short Chain Acyl-CoA Dehydrogenase (SCAD) Deficiency, Short Chain L-3-Hydroxyacyl-CoA Dehydrogenase (SCHAD) Deficiency, Electron Transfer Flavoprotein (ETF) Dehydrogenase Deficiency (GAII & MADD), 3-Hydroxy-3 Methylglutaryl-CoA Lyase Deficiency (HMG), Unclassified FODs)

Fetal Alcohol Support Network (Fetal Alcohol Syndrome)

FG Syndrome Family Alliance (FG Syndrome)

Focus Families (Optic Nerve Hypoplasia- ONH, Septo-optic Dysplasia- SOD)

Foundation Fighting Blindness (Canada) (Retinal Disorders, Laurence-Moon-Biedl-Bardet Syndrome, Night Blindness, Retinitis Pigmentosa, Rod Cone Dystrophy, Usher Syndrome)

Foundation Fighting Blindness (Retinal Disorders, Laurence-Moon-Biedl-Bardet Syndrome, Night Blindness, Retinitis Pigmentosa, Rod Cone Dystrophy, Usher Syndrome)

Foundation for Ichthyosis and Related Skin Types(F.I.R.S.T.) - (Darier Disease, Ichthyosis, Epidermal Nevus Syndrome, Lamellar Ichthyosis, Epidermolytic Hyperkeratosis)

Foundation for Nager and Miller Syndromes (FNMS) (Nager Syndrome, Miller Syndrome)

Foundation for Prader-Willi Research, Canada (FPWRC) (Prader-Willi Syndrome)

Fragile X Research Foundation of Canada (Fragile X)

Freeman-Sheldon Parent Support Group (Freeman-Sheldon Syndrome, Cranio-Carpal-Tarsal Dysplasia, Whistling Face Syndrome)

Friends of Landau-Kleffner Syndrome (FOLKS) (Landau-Kleffner Syndrome)