eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | neuropathy, peripheral |
| Symptom | C0278134|sensory loss |
| Sentences | 4 |
| PubMedID- 21618344 | Hereditary sensory and autonomic neuropathy type i (hsan-i) is an axonal peripheral neuropathy leading to progressive distal sensory loss and severe ulcerations. |
| PubMedID- 20920666 | Hereditary sensory and autonomic neuropathy type i (hsan-i) is an axonal peripheral neuropathy associated with progressive distal sensory loss and severe ulcerations. |
| PubMedID- 24187619 | Grade 4 peripheral neuropathy with nociceptive sensory loss was a painful complication reported in a patient in folfox7. |
| PubMedID- 21307380 | Routine assessments independently coded in the research chart included detailed history (sex, ethnicity, history of diabetes-related complications, and categories of current therapies), physical examination (blood pressure, heart rate, and clinical evaluation for sensory loss consistent with peripheral neuropathy using the 5.07 ), and laboratory assessments (hba1c using the dcct-aligned dca 2000+ urine albumin-to-creatinine ratio and lipid panel performed at the local laboratory). |
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