PedAM
Pediatric Disease Annotations & Medicines
| Disease | glomerulosclerosis |
| Phenotype | C0751778|progressive myoclonus epilepsy |
| Sentences | 1 |
| PubMedID- 21738487 | Limp-2 deficiency causes the autosomal-recessive disorder action myoclonus-renal failure syndrome (amrf), which combines renal glomerulosclerosis with progressive myoclonus epilepsy associated with storage material in the brain [34]. |
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