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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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ConditionThis summary box displays a gene, condition, or laboratory matching your search query. | H syndrome |
| Synonyms: Asrar Facharzt Haque syndrome; FAISALABAD HISTIOCYTOSIS; HISTIOCYTOSIS AND LYMPHADENOPATHY WITH OR WITHOUT CUTANEOUS, CARDIAC, AND/OR ENDOCRINE FEATURES, JOINT CONTRACTURES, AND/OR DEAFNESS; HYPERPIGMENTATION, CUTANEOUS, WITH HYPERTRICHOSIS, HEPATOSPLENOMEGALY, HEART ANOMALIES, AND HYPOGONADISM WITH OR WITHOUT HEARING LOSS; Histiocytosis with joint contractures and sensorineural deafness; Histiocytosis-lymphadenopathy plus syndrome; Hyperpigmentation, Cutaneous, with Hypertrichosis, Hepatosplenomegaly, Heart Anomalies, Hearing Loss, and Hypogonadism; PIGMENTED HYPERTRICHOSIS WITH INSULIN-DEPENDENT DIABETES MELLITUS; Pigmented hypertrichosis and insulin-dependent diabetes mellitus; ROSAI-DORFMAN DISEASE, FAMILIAL; SINUS HISTIOCYTOSIS AND MASSIVE LYMPHADENOPATHY Gene: SLC29A3 |
Labs matching your search
22 labs with tests matching your search, 2 labs matching in other ways
Results:
73 genetic tests from 22 labs with tests matching your search, 2 labs matching in other ways
| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods | |
|---|---|---|---|---|
SLC29A3 Gene Histiocytosis-lymphadenopathy plus syndrome NGS Genetic DNA Test | 1 | 1 |
| |
| 1 | 1 |
| ||
| 1 | 1 |
| ||
| 1 | 1 |
| ||
Histiocytosis-lymphadenopathy plus syndrome (sequence analysis of SLC29A3 gene) | 1 | 1 |
| |
Histiocytosis-Lymphadenopathy Plus Syndrome (SLC29A3 Single Gene Test) | 1 | 1 |
| |
| 3 | 43 |
| ||
| 182 | 117 |
| ||
| 374 | 386 |
| ||
Multigene panel for skeletal dysplasia based on whole-exome sequencing | 1 | 474 |
| |
Multigene panel for autoinflammatory syndromes based on whole-exome sequencing | 1 | 101 |
| |
Multigene panel for hearing loss based on whole-exome sequencing | 1 | 222 |
| |
Multigene panel for primary immunodeficiencies based on whole-exome sequencing | 1 | 535 |
| |
| 1 | 318 |
| ||
| 1 | 200 |
| ||
| 754 | 562 |
| ||
| 405 | 219 |
| ||
| 624 | 349 |
| ||
| 3 | 1969 |
| ||
| 223 | 154 |
|
73 tests from 22 labs
Page 1 of 4❯Histiocytosis-lymphadenopathy plus syndrome, 602782, Autosomal recessive (H syndrome) (SLC29A3 gene) (Sequence Analysis-All Coding Exons) (Postnatal) by Intergen Genetics and Rare Diseases Diagnosis Center
1 condition, 1 gene
1 condition, 1 gene
Histiocytosis-lymphadenopathy plus syndrome, 602782, Autosomal recessive (H syndrome) (SLC29A3 gene) (Sequence Analysis-All Coding Exons) (Prenatal) by Intergen Genetics and Rare Diseases Diagnosis Center
1 condition, 1 gene
1 condition, 1 gene
SLC29A3 Single Gene by Fulgent Genetics
1 condition, 1 gene
1 condition, 1 gene
Histiocytosis-lymphadenopathy plus syndrome (sequence analysis of SLC29A3 gene) by CGC Genetics, Unilabs
1 condition, 1 gene
1 condition, 1 gene
Neonatal Diabetes Panel by Genetic Services Laboratory, University of Chicago
3 conditions, 43 genes
3 conditions, 43 genes
Autoinflammatory Gene Panel by Mayo Clinic Laboratories, Mayo Clinic
182 conditions, 117 genes
182 conditions, 117 genes
Inborn Errors of Immunity GenePanel by Mayo Clinic Laboratories, Mayo Clinic
374 conditions, 386 genes
374 conditions, 386 genes
Multigene panel for skeletal dysplasia based on whole-exome sequencing by CGPP - Center for Predictive and Preventive Genetics, IBMC - Institute for Cell and Molecular Biology
1 condition, 474 genes
1 condition, 474 genes
Multigene panel for autoinflammatory syndromes based on whole-exome sequencing by CGPP - Center for Predictive and Preventive Genetics, IBMC - Institute for Cell and Molecular Biology
1 condition, 101 genes
1 condition, 101 genes
Multigene panel for hearing loss based on whole-exome sequencing by CGPP - Center for Predictive and Preventive Genetics, IBMC - Institute for Cell and Molecular Biology
1 condition, 222 genes
1 condition, 222 genes
Multigene panel for primary immunodeficiencies based on whole-exome sequencing by CGPP - Center for Predictive and Preventive Genetics, IBMC - Institute for Cell and Molecular Biology
1 condition, 535 genes
1 condition, 535 genes
Genomic Unity® Hearing Loss Disorders Analysis by Variantyx, Inc.
1 condition, 318 genes
1 condition, 318 genes
AudioloGene Hearing Loss Panel by Mayo Clinic Laboratories, Mayo Clinic
1 condition, 200 genes
1 condition, 200 genes
Invitae Inborn Errors of Immunity and Cytopenias Panel by Labcorp Genetics (formerly Invitae), LabCorp
754 conditions, 562 genes
754 conditions, 562 genes
Invitae Comprehensive Deafness Panel by Labcorp Genetics (formerly Invitae), LabCorp
405 conditions, 219 genes
405 conditions, 219 genes
Invitae Skeletal Disorders Panel by Labcorp Genetics (formerly Invitae), LabCorp
624 conditions, 349 genes
624 conditions, 349 genes
qGenEx Intellectual disability by Quantitative Genomic Medicine Laboratories, SL
3 conditions, 1969 genes
3 conditions, 1969 genes
Invitae Autoinflammatory and Autoimmunity Syndromes Panel by Labcorp Genetics (formerly Invitae), LabCorp
223 conditions, 154 genes
223 conditions, 154 genes
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.