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Results: 1 to 20 of 42

Tests names and labsConditionsGenes, analytes, and microbesMethods

Congenital Fibrinogen Disorders, FGA, FGB, and FGG Genes, Full Gene Next-Generation Sequencing

Mayo Clinic Laboratories Mayo Clinic
United States
43
  • C Sequence analysis of the entire coding region

PlateletGenex Functional Defect Panel (31 genes) (2 Day STAT TAT)

Machaon Diagnostics
United States
2631
  • C Sequence analysis of the entire coding region

FGA - NGS including CNV analysis

Centogene AG - the Rare Disease Company
Germany
31
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

FGB - NGS including CNV analysis

Centogene AG - the Rare Disease Company
Germany
21
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

FGG - NGS including CNV analysis

Centogene AG - the Rare Disease Company
Germany
21
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

CentoImmuno Panel

Centogene AG - the Rare Disease Company
Germany
323329
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Blood Coagulation Panel

Centogene AG - the Rare Disease Company
Germany
110112
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

CentoICU Panel

Centogene AG - the Rare Disease Company
Germany
829848
  • C Sequence analysis of the entire coding region

Stroke, Cerebral Hemorrhage, Hemiplegia, and Migraine Panel

PreventionGenetics, part of Exact Sciences
United States
345159
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Dysfibrinogenemia Genetic Panel (2 Day STAT TAT)

Machaon Diagnostics
United States
23
  • C Sequence analysis of the entire coding region

Hypofibrinogenemia, congenital, 202400, Autosomal recessive (Congenital fibrinogen deficiency) (FGG gene) (Sequence Analysis-All Coding Exons) (Prenatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Hypofibrinogenemia, congenital, 202400, Autosomal recessive (Congenital fibrinogen deficiency) (FGG gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Hypofibrinogenemia, congenital, 202400, Autosomal recessive (Familial hypodysfibrinogenemia) (FGB gene) (Sequence Analysis-All Coding Exons) (Prenatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Hypofibrinogenemia, congenital, 202400, Autosomal recessive (Familial hypodysfibrinogenemia) (FGB gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Afibrinogenemia, congenital, 202400, Autosomal recessive (Congenital fibrinogen deficiency) (FGG gene) (Sequence Analysis-All Coding Exons) (Prenatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Afibrinogenemia, congenital, 202400, Autosomal recessive (Familial afibrinogenemia) (FGB gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Afibrinogenemia, congenital, 202400, Autosomal recessive (Congenital fibrinogen deficiency) (FGG gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Afibrinogenemia, congenital, 202400, Autosomal recessive (Congenital fibrinogen deficiency) (FGA gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Afibrinogenemia, congenital, 202400, Autosomal recessive (Congenital fibrinogen deficiency) (FGA gene) (Sequence Analysis-All Coding Exons) (Prenatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Afibrinogenemia, congenital, 202400, Autosomal recessive (Familial afibrinogenemia) (FGB gene) (Sequence Analysis-All Coding Exons) (Prenatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 42

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