Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B0e6c018d4ef40e0f0dab5a07f1a1cdd3> ?p ?o ?g. }
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- B0e6c018d4ef40e0f0dab5a07f1a1cdd3 hasDbXref "Orphanet:64751" @default.
- B0e6c018d4ef40e0f0dab5a07f1a1cdd3 type Axiom @default.
- B0e6c018d4ef40e0f0dab5a07f1a1cdd3 annotatedProperty IAO_0000115 @default.
- B0e6c018d4ef40e0f0dab5a07f1a1cdd3 annotatedSource MONDO_0010877 @default.
- B0e6c018d4ef40e0f0dab5a07f1a1cdd3 annotatedTarget "Hereditary motor and sensory neuropathy type 5 is a rare axonal hereditary motor and sensory neuropathy characterized by slowly progressive distal muscle weakness and atrophy with or without sensory loss resulting in difficulty in walking, foot drop and pes cavus, that may be associated with pyramidal signs (extensor plantar responses, mild increase in tone, brisk tendon reflexes), muscle cramps, pain and spasticity." @default.