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Genetic Disorders
Taxonomy Code: YF-3000.3280
Any of a number of illnesses or conditions that are the direct result of the mutation of one or more genes. Some genetic disorders are hereditary, transmitted from parent to offspring, but others occur spontaneously and are not familial in origin.
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Wolman's Disease (YF-3000.9720)
Wilson's Disease (YF-3000.9440)
Tuberous Sclerosis (YF-3000.8780)
Tay-Sachs Disease (YF-3000.8400)
Stickler Syndrome (YF-3000.8125)
Spinal Muscular Atrophy (YF-3000.8098)
Smith-Magenis Syndrome (YF-3000.8010)
Retinoblastoma (YF-3000.7200)
Retinitis Pigmentosa (YF-3000.7160)
Primary Immune Deficiency Disorders (YF-3000.6850)
Phenylketonuria (YF-3000.6380)
Phelan-McDermid Syndrome (YF-3000.6372)
Otosclerosis (YF-3000.5960)
Osteopsathyrosis (YF-3000.5920)
Osteogenesis Imperfecta (YF-3000.5800)
Organic Acidemias (YF-3000.5750)
Ollier's Disease (YF-3000.5740)
Niemann-Pick Disease (YF-3000.5600)
Muscular Dystrophy (YF-3000.5200)
Mucopolysaccharidosis (YF-3000.5100)
Marfan Syndrome (YF-3000.4910)
Maple Syrup Urine Disease (YF-3000.4900)
Lowe's Syndrome (YF-3000.4740)
Huntington's Disease (YF-3000.3720)
Hemorrhagic Telangiectasia (YF-3000.3580)
Hemophilia (YF-3000.3560)
Gout (YF-3000.3400)
Galactosemia (YF-3000.3200)
Fragile X Syndrome (YF-3000.3180)
Farber Disease (YF-3000.3100)
Fabry's Disease (YF-3000.3070)
Epidermolysis (YF-3000.3030)
Ehlers-Danlos Syndrome (YF-3000.2760)
Ectodermal Dysplasias (YF-3000.2720)
Dysautonomia (YF-3000.2640)
Dup15q Syndrome (YF-3000.2585)
Doose Syndrome (YF-3000.2550)
Cri Du Chat Syndrome (YF-3000.2220)
Coffin-Lowry Syndrome (YF-3000.1850)
Charcot-Marie Tooth Disease (YF-3000.1700)
Angelman Syndrome (YF-3000.0587)
Thalassemia (YF-3000.0560-850)
Sickle Cell Anemia (YF-3000.0560-800)
Aicardi Syndrome (YF-3000.0265)