eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | pendred syndrome |
| Symptom | C1384666|hearing loss |
| Sentences | 1 |
| PubMedID- 22429511 | Objective: recessive mutations of the slc26a4 (pds) gene on chromosome 7q31 can cause sensorineural hearing loss with goiter (pendred syndrome) or non-syndromic autosomal recessive hearing loss (dfnb4). |
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