eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | kid syndrome |
| Symptom | C0018784|sensorineural hearing loss |
| Sentences | 1 |
| PubMedID- 25575739 | (2004), who described a case of kid syndrome with sensorineural hearing loss and congenital atrichia caused by mutation in the gene gjb6 (cx30), which is usually connected with clouston syndrome. |
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