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New filters have been added to narrow your search: Test target, to filter by number of genes; Genes and Conditions, to search by gene symbol or condition name; and Labs, to search by a laboratory name.
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Labs matching your search
29 labs with tests matching your search, 3 labs matching in other ways
Results:
140 genetic tests from 29 labs with tests matching your search, 3 labs matching in other ways
| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods | |
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| 7 | 41 |
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Hemophagocytic Lymphohistiocytosis Panel by next generation sequencing (NGS) | 18 | 18 |
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Invitae Hereditary Hemophagocytic Lymphohistiocytosis (HLH) Disorders Panel | 37 | 24 |
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Hemophagocytic lymphohistiocytosis, familial: Full gene sequencing panel | 5 | 5 |
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| 29 | 29 |
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140 tests from 29 labs
Page 1 of 7❯Hemophagocytic lymphohistiocytosis, familial, 3, 608898; FHL3 (Familial hemophagocytic lymphohistiocytosis) (UNC13D gene) (Sequence Analysis-All Coding Exons) (Postnatal) by Intergen Genetics and Rare Diseases Diagnosis Center
1 condition, 1 gene
1 condition, 1 gene
Hemophagocytic lymphohistiocytosis, familial, 2, 603553, Autosomal recessive; FHL2 (Familial hemophagocytic lymphohistiocytosis) (PRF1 gene) (Sequence Analysis-All Coding Exons) (Postnatal) by Intergen Genetics and Rare Diseases Diagnosis Center
1 condition, 1 gene
1 condition, 1 gene
Hemophagocytic lymphohistiocytosis, familial, 2, 603553, Autosomal recessive; FHL2 (Familial hemophagocytic lymphohistiocytosis) (MLPA) by Intergen Genetics and Rare Diseases Diagnosis Center
1 condition, 1 gene
1 condition, 1 gene
Hemophagocytic lymphohistiocytosis, familial, 2, 603553, Autosomal recessive; FHL2 (Familial hemophagocytic lymphohistiocytosis) (PRF1 gene) (Sequence Analysis-All Coding Exons) (Prenatal) by Intergen Genetics and Rare Diseases Diagnosis Center
1 condition, 1 gene
1 condition, 1 gene
Hemophagocytic lymphohistiocytosis, familial, 2, 603553, Autosomal recessive; FHL2 (Familial hemophagocytic lymphohistiocytosis) (Prenatal) (MLPA) by Intergen Genetics and Rare Diseases Diagnosis Center
1 condition, 1 gene
1 condition, 1 gene
Hemophagocytic lymphohistiocytosis, familial, 4, 603552, Autosomal recessive; FHL4 (Familial hemophagocytic lymphohistiocytosis) (Prenatal) (MLPA) by Intergen Genetics and Rare Diseases Diagnosis Center
1 condition, 1 gene
1 condition, 1 gene
Hemophagocytic lymphohistiocytosis, familial, 3, 608898; FHL3 (Familial hemophagocytic lymphohistiocytosis) (Prenatal) (MLPA) by Intergen Genetics and Rare Diseases Diagnosis Center
1 condition, 1 gene
1 condition, 1 gene
Hemophagocytic lymphohistiocytosis, familial, 4, 603552, Autosomal recessive; FHL4 (Familial hemophagocytic lymphohistiocytosis) (MLPA) by Intergen Genetics and Rare Diseases Diagnosis Center
1 condition, 1 gene
1 condition, 1 gene
Hemophagocytic lymphohistiocytosis, familial, 3, 608898; FHL3 (Familial hemophagocytic lymphohistiocytosis) (UNC13D gene) (Sequence Analysis-All Coding Exons) (Prenatal) by Intergen Genetics and Rare Diseases Diagnosis Center
1 condition, 1 gene
1 condition, 1 gene
Hemophagocytic lymphohistiocytosis, familial, 3, 608898; FHL3 (Familial hemophagocytic lymphohistiocytosis) (MLPA) by Intergen Genetics and Rare Diseases Diagnosis Center
1 condition, 1 gene
1 condition, 1 gene
Hemophagocytic lymphohistiocytosis, familial, 5, 613101; FHL5 (Familial hemophagocytic lymphohistiocytosis) (STXBP2 gene) (Sequence Analysis-All Coding Exons) (Prenatal) by Intergen Genetics and Rare Diseases Diagnosis Center
1 condition, 1 gene
1 condition, 1 gene
Hemophagocytic lymphohistiocytosis, familial, 5, 613101; FHL5 (Familial hemophagocytic lymphohistiocytosis) (STXBP2 gene) (Sequence Analysis-All Coding Exons) (Postnatal) by Intergen Genetics and Rare Diseases Diagnosis Center
1 condition, 1 gene
1 condition, 1 gene
Hemophagocytic lymphohistiocytosis, familial, 4, 603552, Autosomal recessive; FHL4 (Familial hemophagocytic lymphohistiocytosis) (STX11 gene) (Sequence Analysis-All Coding Exons) (Prenatal) by Intergen Genetics and Rare Diseases Diagnosis Center
1 condition, 1 gene
1 condition, 1 gene
Hemophagocytic lymphohistiocytosis, familial, 4, 603552, Autosomal recessive; FHL4 (Familial hemophagocytic lymphohistiocytosis) (STX11 gene) (Sequence Analysis-All Coding Exons) (Postnatal) by Intergen Genetics and Rare Diseases Diagnosis Center
1 condition, 1 gene
1 condition, 1 gene
Hemophagocytic Lymphohistiocytosis Panel by next generation sequencing (NGS) by Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory, Cincinnati Children's Hospital Medical Center
18 conditions, 18 genes
18 conditions, 18 genes
Invitae Hereditary Hemophagocytic Lymphohistiocytosis (HLH) Disorders Panel by Labcorp Genetics (formerly Invitae), LabCorp
37 conditions, 24 genes
37 conditions, 24 genes
Hemophagocytic lymphohistiocytosis, familial: Full gene sequencing panel by CEN4GEN Institute for Genomics and Molecular Diagnostics
5 conditions, 5 genes
5 conditions, 5 genes
Familial Hemophagocytic Lymphohistiocytosis (FHL) Panel by PreventionGenetics, part of Exact Sciences
29 conditions, 29 genes
29 conditions, 29 genes
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