قابل توجه کسانی که سابقه بیماری رنتیکی در خانواده خود دارند
با استفاده از روش ای وی اف میتوان از عدم انتقال بیماریهای زنتیکی زیر به جنین اطمینان حاصل کرد
Achondroplasia Adenosine Deaminase Deficiency Adrenal Hyperplasia Alagille Syndrome Albinism Alpha Thalassemia Ataxia Telangectasia Auto-immune Lymphoprolepherative Syndrome Beckwith-Wiedernmann Syndrome Beta Thalassemia, Sickle Cell Anemia Bilateral Lebers Congenital Amaurosis Biotidinase Deficiency Blindness (Usher syndrome) Brakytachtyly Type B CADASIL Carbohydrate-Deficient Glycoprotein Syndrome, Type I Charcot-marie Tooth Disease Congenitail Adrenal Hyperplasia Congenitail Cholestosis Congenital Analgesia Syndrome Congenital Disorder of Glycosylation Congenital Icthysosis Congenital Mytonia Congenital Nephrosis Criggler Najjar Syndrome Cystic Fibrosis Deafness (Connexin 26) Duchenne Backet Muscular Dystrophy Ehler Donlos Syndrome Epidermolysis Bullosa Fabrys Disease Familial Juvenile Nephrosis Familial Meditteranian Fever Disease Fanconi Anemia Fragile X Syndrome Friedreich Ataxia Fructose 1,6 Biphosphate Glucose 6 Phosphate Dehydrogenase Gaucher Disease Glutaric Aciduria type1,2,3 Glycosyl Decarboxylase (GLDC,AMH) Hemachromatosis Hemophilia Heraditary Spastic Paraparesis Huler-schei Syndrome Hurler Syndrome (Type 1) Hyperoxaluria Icythyosis Infartile Polycystic Kidney Disease Insulin-Dependent Diabetes Mellitus (type 1 diabetus mellitus) Isovaleric Aciduria Joubert Syndrome K-Ras Mutation screening Lamellar Ichosis Leucodystrophia Leukocyte Adhesion syndrome Lipoprotein lipase syndrome Maple Syrup Urine Disease Marfan Syndrome Maturity-onset diabetes of the young Meckel Gruber Syndrome Medium Chain acyl CoA Dehydrogenase Methylene Tetrahydrofolate Reductase Methylmalonic Acidemia Mitochondrial genome screening Mucopolysaccharidosis TYPE I Mucopolysaccharidosis-Type III Mucopolysaccharidosis-Type IV Mucopolysaccharidosis-Type VI Multiple Acyl coA deficiency Multiple Endocrine Neoplasia-Type1 Neiman-pick Type B Neonatal Cholestasis Neurofibromatosis Neuronal Ceroid Lipopherosis Nevoid Basal Cell Carcinoma Syndrome Non Polyposis Colon Cancer Non-Insulin Dependent Diabetes Noonan Syndrome Omenn Syndrome Ornithine Transcarbomylase Deficiency Osteogenesis Imperfecta Osteopetrosis Paroxymal Biogene Disorder Perforin PhenylKetonuria Polycythemia Vera Pompe Disease Prader Weely Syndrome Primary Dystonia Pseudohypoparathyrosis Retinitis Pigmentaris Rett Syndrome Sandhoff Disease Sanjad Sakaty Seckel Disease Short Chain acyl CoA Dehydrogenase Skeletal Dysplasia Smith lemli optiz syndrome Spina Bifida Spinal Muscular Atrophy Thanatophoric Dysplasia Thrombcytopenia Tuberous Sclerosis Very Long Chain acyl CoA Dehydrogenase Vitamin D Receptors Wilson disease X-Linked Deafness X-linked thrombocytopenia Y-chromosome Micro Deletion