RareMap
Understand hidden genetic factors and get comprehensive insights into rare inherited conditions
Alpha Thalassemia
Learn about alpha thalassemia, its genetic causes, symptoms, and the importance of early diagnosis. Explore MapmyGenome's advanced genetic testing and personalized management solutions for effective care and family planning.
Beta Thalassemia
Discover comprehensive insights on Beta Thalassemia, an inherited blood disorder. Learn about its symptoms, genetic testing, and how MapmyGenome's screening can help you assess your risk and make informed family planning decisions.
Cystic Fibrosis
Discover comprehensive cystic fibrosis (CF) screening with MapmyGenome. Learn about CF, its impact on health, and the importance of early detection and carrier screening. Get accurate results and expert guidance for better health outcomes.
Duchenne Muscular Dystrophy
Explore Duchenne muscular dystrophy (DMD) screening with MapmyGenome. Learn about DMD, its symptoms, and the importance of genetic testing for accurate diagnosis and personalized management. Access expert guidance and carrier screening for informed family planning.
Fatty Acid Oxidation Disorders
Discover insights into Fatty Acid Oxidation Disorders (FAODs), including causes, symptoms, and management strategies. Learn about the importance of early detection, testing, and how MapmyGenome supports families with comprehensive genetic testing and personalized care.
Huntingtons Disease
Explore comprehensive Huntington’s disease (HD) screening with MapmyGenome. Learn about HD, its symptoms, and the importance of early detection and personalized management. Access expert genetic testing and counseling to support better health outcomes.
Lysosomal Storage Disorders
Discover essential information about Lysosomal Storage Disorders (LSDs), including their causes, symptoms, and management options. Learn how early diagnosis and personalized care from MapmyGenome can improve outcomes for affected individuals.
MTHFR Gene Polymorphism
Explore MTHFR genetic testing to understand your risk for cardiovascular diseases, blood clotting disorders, pregnancy complications, and medication responses. Learn how MTHFR variants impact your health and discover personalized recommendations with MapmyGenome.
Pro-thrombin and Factor V Leiden
Discover your genetic risk for blood clots with Prothrombin and Factor V Leiden testing. Learn how this test can help prevent DVT, PE, and other clot-related complications.
SCID
Learn about Severe Combined Immunodeficiency (SCID) with MapmyGenome. Discover the causes, symptoms, and importance of genetic testing for early diagnosis and personalized management of this life-threatening immune disorder.
Sickle Cell Anemia
Explore our comprehensive guide on sickle cell anemia, including detailed explanations, clinical utility, testing recommendations, and MapmyGenome's offerings. Understand the impact of this genetic disorder and how early diagnosis can improve outcomes.
Skeletal Dysplasia
Explore Skeletal Dysplasia with MapmyGenome. Learn about the causes, symptoms, and the importance of genetic testing for accurate diagnosis and personalized management of this rare genetic bone disorder.
Spinal Muscular Atrophy
Explore Spinal Muscular Atrophy (SMA) with MapmyGenome. Learn about the causes, symptoms, and the importance of genetic testing using MLPA for early diagnosis and management of this critical genetic disorder.
Spinocerebellar Ataxia(SCA)
Comprehensive genetic testing options using multiple techniques for SCA to help with accurate diagnosis and personalized care to address any future coordination or movement diffuculties.
Urea Cycle Disorders
Learn about Urea Cycle Disorders (UCDs), their diagnosis, clinical utility, and genetic testing options at MapmyGenome. Discover how early detection and management can improve patient outcomes.