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- Ba525e28f60dbffd21a4b078e98d359dc hasDbXref "Orphanet:100046" @default.
- Ba525e28f60dbffd21a4b078e98d359dc type Axiom @default.
- Ba525e28f60dbffd21a4b078e98d359dc annotatedProperty IAO_0000115 @default.
- Ba525e28f60dbffd21a4b078e98d359dc annotatedSource MONDO_0011909 @default.
- Ba525e28f60dbffd21a4b078e98d359dc annotatedTarget "Autosomal dominant intermediate Charcot-Marie-Tooth disease type D is a rare hereditary motor and sensory neuropathy characterized by intermediate motor median nerve conduction velocities (usually between 25 and 45 m/s) and signs of both axonal degeneration and demyelination without onion bulbs in nerve biopsies. It presents with usual Charcot-Marie-Tooth disease clinical features of variable severity (progressive muscle weakness and atrophy of the distal extremities, distal sensory loss, reduced or absent deep tendon reflexes, and feet deformities). Other findings in some of the families include debilitating neuropathic pain and mild postural/kinetic upper limb tremor." @default.