eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | hartnup disease |
| Comorbidity | C0027813|neuritis |
| Sentences | 2 |
| PubMedID- 21764587 | We report the development of sequential demyelinating optic neuritis in a patient with genetically confirmed charcot-marie-tooth disease type 1a, a hereditary neuropathy. |
| PubMedID- 25883554 | (2003) to staging pd according to appearance of α-synuclein containing lbs and lewy neuritis with disease severity. |
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