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loading...| Preferred Name |
Hypertensive Nephropathy |
| ID |
http://purl.bioontology.org/ontology/MESH/C563161 |
| cui |
C0848548 |
| HM |
D006977 D009393 |
| Inverse of RB |
0 |
| Mapped to | |
| MDA |
20121105 |
| MeSH Frequency |
220 |
| MMR |
20150818 |
| notation |
C563161 |
| prefLabel |
Hypertensive Nephropathy |
| SC |
3 |
| Scope Statement |
A hereditary disorder reported in an AFRICAN AMERICAN family. Nearly half of those affected had CHRONIC KIDNEY FAILURE and HYPERTENSION. PROTEINURIA and focal segmental glomerular sclerosis-like lesions (OMIM: 603278) with ARTERIOLE thickening were observed in one patient. Has been mapped to chromosome 9. OMIM: 608026 |
| TERMUI |
T802320 |
| TH |
OMIM (2013) |
| tui |
T047 |
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