eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | hereditary neuropathy with liability to pressure palsies |
| Comorbidity | C0007959|charcot-marie-tooth disease |
| Sentences | 1 |
| PubMedID- 21252112 | Missense or nonsense mutations also cause more severe charcot-marie-tooth disease type 1a forms of infancy or hereditary neuropathy with liability to pressure palsies, but they are presumably very rare. |
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