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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
53 labs with tests matching your search, 3 labs matching in other ways
Results:
169 genetic tests from 53 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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MVK Gene Porokeratosis type 3, disseminated superficial actinic NGS Genetic DNA Test | 1 | 1 |
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| 7 | 41 |
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169 tests from 53 labs
Page 1 of 9❯MVK by Institute for Human Genetics, University Medical Center Freiburg
3 conditions, 1 gene
3 conditions, 1 gene
MVK by Institute of Human Genetics, Medical University Innsbruck
3 conditions, 1 gene
3 conditions, 1 gene
MVK by Genome Diagnostics Laboratory, University Medical Center Utrecht
1 condition, 1 gene
1 condition, 1 gene
MVK Gene Mevalonic aciduria NGS Genetic DNA Test by DNA Labs India
1 condition, 1 gene
1 condition, 1 gene
MVK Sequencing by Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory, Cincinnati Children's Hospital Medical Center
3 conditions, 1 gene
3 conditions, 1 gene
Hyper-IgD syndrome, 260920, Autosomal recessive; HIDS (Hyperimmunoglobulinemia D with periodic fever) (MVK gene) (Sequence Analysis-All Coding Exons) (Postnatal) by Intergen Genetics and Rare Diseases Diagnosis Center
1 condition, 1 gene
1 condition, 1 gene
Hyper-IgD syndrome, 260920, Autosomal recessive; HIDS (Hyperimmunoglobulinemia D with periodic fever) (MVK gene) (Sequence Analysis-All Coding Exons) (Prenatal) by Intergen Genetics and Rare Diseases Diagnosis Center
1 condition, 1 gene
1 condition, 1 gene
Mevalonic aciduria, 610377, Autosomal recessive; MEVA (Mevalonic aciduria) (MVK gene) (Sequence Analysis-All Coding Exons) (Postnatal) by Intergen Genetics and Rare Diseases Diagnosis Center
1 condition, 1 gene
1 condition, 1 gene
Mevalonic aciduria, 610377, Autosomal recessive; MEVA (Mevalonic aciduria) (MVK gene) (Sequence Analysis-All Coding Exons) (Prenatal) by Intergen Genetics and Rare Diseases Diagnosis Center
1 condition, 1 gene
1 condition, 1 gene
Porokeratosis 3, multiple types, 175900, Autosomal dominant; POROK3 (Porokeratosis of Mibelli) (MVK gene) (Sequence Analysis-All Coding Exons) (Postnatal) by Intergen Genetics and Rare Diseases Diagnosis Center
1 condition, 1 gene
1 condition, 1 gene
MVK Single Gene by Fulgent Genetics
3 conditions, 1 gene
3 conditions, 1 gene
Sanger sequencing of MVK by Laboratorio de Genetica Clinica SL
1 condition, 1 gene
1 condition, 1 gene
Sanger sequencing of MVK by Laboratorio de Genetica Clinica SL
1 condition, 1 gene
1 condition, 1 gene
MVK single gene sequencing by Molecular Vision Laboratory
3 conditions, 1 gene
3 conditions, 1 gene
Hiper IgD syndrome (sequence analysis of MVK gene) by CGC Genetics, Unilabs
1 condition, 1 gene
1 condition, 1 gene
Mevalonate Kinase Deficiency (MVK Single Gene Test) by Fulgent Genetics
3 conditions, 1 gene
3 conditions, 1 gene
Single gene testing MVK by CeGaT GmbH
3 conditions, 1 gene
3 conditions, 1 gene
Hyperimmunoglobulin D with periodic fever by Department of Clinical Immunology, Odense University Hospital
1 condition, 1 gene
1 condition, 1 gene
IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.