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Metabolic Diseases

Mikrogen > Genetic Tests > Metabolic Diseases
Metabolic Diseases

MODY Type 6

Metabolic Diseases

MODY Type 5

Metabolic Diseases

MODY Type 4

Metabolic Diseases

MODY Type 3

Metabolic Diseases

MODY Type 2

Metabolic Diseases

MODY Type 1

Metabolic Diseases

Methyl malonic acidemia

Metabolic Diseases

Metachromatic Leukodystrophy

Metabolic Diseases

Menkes Syndrome

Metabolic Diseases

Mapple Urine Syrup (MSUD) Type 1B

Metabolic Diseases

Mapple Urine Syrup (MSUD) Type 1A

Metabolic Diseases

Carnitine Palmitoyltransferase 2 Deficiency

Metabolic Diseases

Hypertriglyceridemia LIPI Gene

Metabolic Diseases

Hyperoxaluria Type 1 (AGXT Gene)

Metabolic Diseases

hyperinsulinemia

Metabolic Diseases

Hyperimmunoglobulin D Syndrome (HIDS)

Metabolic Diseases

Hemochromatosis HFE Whole Gene

Metabolic Diseases

Hemochromatosis TFR2

Metabolic Diseases

Glucose – 6 – Phosphate Dehydrogenase Deficiency

Metabolic Diseases

Glucose Galactose Malabsorption

Metabolic Diseases

Glycogen Storage Disease Type 3

Metabolic Diseases

Glycogen Storage Disease Type 1

Metabolic Diseases

Gangliosidosis Type 1, 2, 3

Metabolic Diseases

galactosemia

Metabolic Diseases

Frataxin – FXN Sequence Analysis

Metabolic Diseases

Fish Eye Disease

Metabolic Diseases

Phenylketonuria Whole Gene

Metabolic Diseases

Fanconi-Bickel Syndrome

Metabolic Diseases

Fabry Disease

Metabolic Diseases

CYP2C19 Polymorphism Screening

Metabolic Diseases

Biotinidase Deficiency

Metabolic Diseases

APOE Genotyping

Metabolic Diseases

Familial Hyperlipidemia

Metabolic Diseases

Glycogen storage disease Ib/c

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Tests

  • Whole Exome / Genome Sequencing
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  • Skeletal, Connective Tissue and Skin Diseases
  • Endocrine Diseases
  • Malformation and Retardation Syndromes
  • Cardiology
  • Prenatal Genetic Tests
  • Immunology

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