Genetic Disorders Directory
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- Hunter Syndrome (MPS II)
- Alpha-1 Antitrypsin (AAT) Deficiency
- Mucopolysaccharidosis I (MPS I)
- Fabry Disease
- Inherited Lipodystrophy
- What Is Gaucher Disease?
- Tuberous Sclerosis Diagnosis, Symptoms, and Treatment
- Pompe Disease: Learn the Details About This Rare Disorder
- What Is Brugada Syndrome?
- Juvenile Macular Degeneration: Stargardt's and Best Disease
- What Is Cat Eye Syndrome?
- What Is Prader-Willi Syndrome?
- Transthyretin Familial Amyloid Polyneuropathy
- Hereditary Angioedema: Causes, Symptoms, and Treatment
- Polycythemia Vera
- Adenosine Deaminase Severe Combined Immunodeficiency (ADA-SCID): Symptoms, Causes, and Treatments
- Cushing Syndrome
- Connective Tissue Disease: Types, Symptoms, Causes