Filters
| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
|---|---|---|---|
Mitochondrial nonsyndromic sensorineural deafness Bioarray Spain | 1 | 1 |
|
mtDNA encoded Mitochondriopathies Panel CeGaT GmbH Germany | 11 | 37 |
|
MGZ Medical Genetics Center Germany | 3 | 8 |
|
Asper Biogene Asper Biogene LLC Estonia | 83 | 79 |
|
Deafness, Hereditary: Mitochondrial DNA mutations analysis (A1555G, C1494T, T1095C) GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases Spain | 1 | 1 |
|
Deafness, Hereditary: GJB2 and OTOF genes and mitochondrial DNA mutations analysis GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases Spain | 4 | 3 |
|
Deafness, Hereditary: GJB2 (Connexin 26) gene y mitochondrial DNA mutations analysis GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases Spain | 3 | 2 |
|
MT-TS1-Related Hearing Loss and Deafness MGZ Medical Genetics Center Germany | 1 | 1 |
|
Hearing Loss/Deafness Multi-Gene Panels MGZ Medical Genetics Center Germany | 2 | 4 |
|
MT-RNR1-Related Hearing Loss and Deafness MGZ Medical Genetics Center Germany | 1 | 1 |
|
Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center United States | 2 | 4 |
|
Hearing impairment (inherited causes) Molecular Diagnosis Centre National University Hospital Singapore | 3 | 4 |
|
MTRNR1-related hearing loss and deafness Institute of Human Genetics Cologne University Germany | 2 | 1 |
|
Aminoglycoside-Induced Hearing Loss: MT-RNR1 Targeted Analysis Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center United States | 1 | 1 |
|
Hearing Loss (Connexin-26, Connexin-30, Mitochondrial A1555G) Center for Human Genetics, Inc United States | 5 | 3 |
|
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