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The Service Tree lists all services in "branched" groups, starting with the very general and moving to the very specific. Click on the name of any group name to see the sub-groups available within it. Click on a service code to see its details and the providers who offer that service.

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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Aicardi Syndrome (YF-3000.0265)

Sickle Cell Anemia (YF-3000.0560-800)

Thalassemia (YF-3000.0560-850)

Angelman Syndrome (YF-3000.0587)

Charcot-Marie Tooth Disease (YF-3000.1700)

Coffin-Lowry Syndrome (YF-3000.1850)

Cri Du Chat Syndrome (YF-3000.2220)

Doose Syndrome (YF-3000.2550)

Dup15q Syndrome (YF-3000.2585)

Dysautonomia (YF-3000.2640)

Ectodermal Dysplasias (YF-3000.2720)

Ehlers-Danlos Syndrome (YF-3000.2760)

Epidermolysis (YF-3000.3030)

Fabry's Disease (YF-3000.3070)

Farber Disease (YF-3000.3100)

Fragile X Syndrome (YF-3000.3180)

Galactosemia (YF-3000.3200)

Gout (YF-3000.3400)

Hemophilia (YF-3000.3560)

Hemorrhagic Telangiectasia (YF-3000.3580)

Huntington's Disease (YF-3000.3720)

Lowe's Syndrome (YF-3000.4740)

Maple Syrup Urine Disease (YF-3000.4900)

Marfan Syndrome (YF-3000.4910)

Mucopolysaccharidosis (YF-3000.5100)

Muscular Dystrophy (YF-3000.5200)

Niemann-Pick Disease (YF-3000.5600)

Ollier's Disease (YF-3000.5740)

Organic Acidemias (YF-3000.5750)

Osteogenesis Imperfecta (YF-3000.5800)

Osteopsathyrosis (YF-3000.5920)

Otosclerosis (YF-3000.5960)

Phelan-McDermid Syndrome (YF-3000.6372)

Phenylketonuria (YF-3000.6380)

Primary Immune Deficiency Disorders (YF-3000.6850)

Retinitis Pigmentosa (YF-3000.7160)

Retinoblastoma (YF-3000.7200)

Smith-Magenis Syndrome (YF-3000.8010)

Spinal Muscular Atrophy (YF-3000.8098)

Stickler Syndrome (YF-3000.8125)

Tay-Sachs Disease (YF-3000.8400)

Tuberous Sclerosis (YF-3000.8780)

Wilson's Disease (YF-3000.9440)

Wolman's Disease (YF-3000.9720)

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