Filters
Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
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X-chromosome High Resolution microarray analysis Pittsburgh Cytogenetics Laboratory University of Pittsburgh Medical Center United States | 240 | 171 |
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Comprehensive Hearing Loss + mtDNA MNG Laboratories (Medical Neurogenetics, LLC.) United States | 218 | 300 |
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Genologica Medica Spain | 6 | 3 |
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Non-syndromic hearing loss panel. 95-gene NGS panel. Genologica Medica Spain | 146 | 94 |
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Hearing Loss, Comprehensive Panel CNH Molecular Diagnostics Laboratory Childrens National Hospital United States | 142 | 84 |
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Deafness, X-linked: Full gene sequencing panel CEN4GEN Institute for Genomics and Molecular Diagnostics Canada | 6 | 6 |
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Comprehensive Hearing Loss NGS Panel Fulgent Genetics United States | 332 | 167 |
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Fulgent Genetics United States | 98 | 43 |
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Nonsyndromic Hearing Loss NGS Panel Fulgent Genetics United States | 146 | 99 |
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Keratitis-ichthyosis-deafness Syndrome (GJB2 Single Gene Test) Fulgent Genetics United States | 8 | 1 |
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Clouston Syndrome (GJB6 Single Gene Test) Fulgent Genetics United States | 5 | 1 |
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Bart-Pumphrey Syndrome (GJB2 Single Gene Test) Fulgent Genetics United States | 8 | 1 |
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Hystrix-like Ichthyosis With Deafness (GJB2 Single Gene Test) Fulgent Genetics United States | 8 | 1 |
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Pachyonychia Congenita NGS Panel Fulgent Genetics United States | 22 | 8 |
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Beacon Expanded Female Carrier Screening Plus Panel Fulgent Genetics United States | 716 | 335 |
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Beacon Expanded Male Carrier Screening Panel Fulgent Genetics United States | 636 | 298 |
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Beacon Expanded Male Carrier Screening Plus Panel Fulgent Genetics United States | 661 | 306 |
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Beacon Expanded Female Carrier Screening Panel Fulgent Genetics United States | 690 | 326 |
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Hearing Loss Advanced Sequencing and CNV Evaluation Athena Diagnostics United States | 249 | 184 |
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DEAFNESS, NON-SYNDROMIC SENSORINEURAL (X-LINKED) Laboratorio de Genetica Clinica SL Spain | 1 | 1 |
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