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- Bebb8c7faed25f4eee89837e1ba3711d4 hasDbXref "Orphanet:83467" @default.
- Bebb8c7faed25f4eee89837e1ba3711d4 type Axiom @default.
- Bebb8c7faed25f4eee89837e1ba3711d4 annotatedProperty IAO_0000115 @default.
- Bebb8c7faed25f4eee89837e1ba3711d4 annotatedSource MONDO_0008718 @default.
- Bebb8c7faed25f4eee89837e1ba3711d4 annotatedTarget "Morvan syndrome is a rare, life-threatening, acquired neurologic disease characterized by neuromyotonia, dysautonomia and encephalopathy with severe insomnia. Signs involving central (e.g. hallucinations, confusion, amnesia, myoclonus), autonomic (e.g. variations in blood pressure, hyperhidrosis) and peripheral (e.g. painful cramps, myokymia) hyperactivity, as well as systemic manifestations (such as weight loss, pruritus, fever), are reported. Thymoma is present in some cases." @default.