PedAM
Pediatric Disease Annotations & Medicines
| Disease | neuropathy |
| Phenotype | C0018801|cardiac failure |
| Sentences | 1 |
| PubMedID- 26243339 | Background: hereditary transthyretin amyloidosis (attr) is usually characterised by a progressive peripheral and autonomic neuropathy often with associated cardiac failure and is due to dominantly inherited transthyretin mutations causing accelerated amyloid deposition. |
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