PedAM
Pediatric Disease Annotations & Medicines
| Disease | glomerulosclerosis |
| Phenotype | C0027719|nephrosclerosis |
| Sentences | 1 |
| PubMedID- 20116156 | Both cases were homozygous for the myh9 e1 risk haplotype, the variant strongly associated with idiopathic fsgs, collapsing fsgs in human immunodeficiency virus-associated nephropathy, and focal global glomerulosclerosis (historically attributed to hypertensive nephrosclerosis). |
Page: 1