| manager |
|
| language |
- |
| license |
- |
| created at |
2024-09-19 07:43:07 UTC |
| updated at |
2024-09-23 18:19:38 UTC |
|
MedGen CUI
Namespace: https://www.ncbi.nlm.nih.gov/medgen/
|
622,528 entries
|
There is 0 pattern entry.
|
UMOD-related kidney disease
|
C4551496 |
|
|
Uromodulin-associated kidney disease
|
C4551496 |
|
|
uromodulin storage disease
|
C4551496 |
|
|
uromodulin-associated kidney disease
|
C4551496 |
|
|
Glomerulocystic kidney disease with hyperuricemia and isosthenuria
|
C4551496 |
|
|
glomerulocystic kidney disease with hyperuricemia and isosthenuria
|
C4551496 |
|
|
tubulointerstitial kidney disease, autosomal dominant, 1
|
C4551496 |
|
|
UMOD-related autosomal dominant tubulointerstitial kidney disease
|
C4551496 |
|
|
Gouty nephropathy, familial juvenile
|
C4551496 |
|
|
hyperuricemic nephropathy, familial juvenile, 1
|
C4551496 |
|
|
hyperuricemic nephropathy, familial juvenile, type 1
|
C4551496 |
|
|
familial juvenile hyperuricaemic nephropathy
|
C4551496 |
|
|
familial juvenile hyperuricemic nephropathy caused by mutation in UMOD
|
C4551496 |
|
|
Familial juvenile hyperuricemic nephropathy type 1
|
C4551496 |
|
|
familial juvenile hyperuricemic nephropathy type 1
|
C4551496 |
|
