Clinical Biochemical Genetics
Biochemical Genetics involves testing and determining inherited metabolic disease, monitoring of treating, and distinguishing heterozygous carriers from non-carriers by metabolite and enzymatic analysis of physiological fluids and tissues in patients. Hereditary metabolic disorders are tested by extremely specialized and fragmented activity, and mostly by research-oriented scientists.
- Inborn errors of metabolism
- Malabsorption
- Malnutrition disorders
Related Conference of Clinical Biochemical Genetics
May 25-26, 2026
35th International Conference on Clinical Diabetes, Diabetic Medication & Treatment
Zurich, Switzerland
June 08-09, 2026
3rd International Congress on Endocrinology and Complications of Diabetes
Rome, Italy
September 23-24, 2026
24th Global Conference on Diabetes, Endocrinology and Primary Healthcare
Paris, France
September 28-29, 2026
25th International Conference on Diabetes, Nutrition, Obesity and Eating Disorders
Berlin, Germany
Clinical Biochemical Genetics Conference Speakers
Recommended Sessions
- Advanced Treatments of Diabetes and Metabolic Syndrome
- Cardio-Metabolic Diseases
- Cholesterol Metabolism
- Clinical Biochemical Genetics
- COVID-19 and Diabetes
- Diabetes and Oral Health
- Diabetes Mellitus and Metabolic Disorders
- Diabetic Education and Healthcare Professionals
- Diabetic Eye Complications
- Diabetic Heart Diseases and Management
- Endocrine Oncology
- Endocrinology
- Gestational Diabetes
- Inherited or Inborn Metabolic Disorders
- Lipid Metabolism
- Medical Devices in Diabetes Treatment
- Medicinal Plants for Metabolic Disorders
- Metabolic Brain Diseases
- Metabolic Liver Diseases
- Metabolic Syndrome
- Metabolism and Metabolic Disorders
- Obesity and Metabolic Disorders
- Pancreas Disorder and Islet Transplantation
- Pediatric Metabolic Disorders
- Prevention & Management of Metabolic Disease
- Reproductive Endocrinology and Infertility
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