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| created at |
2024-09-19 07:43:07 UTC |
| updated at |
2024-09-23 18:19:38 UTC |
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MedGen CUI
Namespace: https://www.ncbi.nlm.nih.gov/medgen/
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622,528 entries
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There is 0 pattern entry.
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autosomal dominant medullary cystic kidney disease type 2
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C4551496 |
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autosomal dominant medullary cystic kidney disease with hyperuricemia
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C4551496 |
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Glomerulocystic kidney disease with hyperuricemia and isosthenuria
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C4551496 |
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glomerulocystic kidney disease with hyperuricemia and isosthenuria
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C4551496 |
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tubulointerstitial kidney disease, autosomal dominant, 1
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C4551496 |
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Gouty nephropathy, familial juvenile
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C4551496 |
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hyperuricemic nephropathy, familial juvenile, 1
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C4551496 |
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hyperuricemic nephropathy, familial juvenile, type 1
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C4551496 |
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autosomal dominant tubulointerstitial kidney disease - UMOD
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C4551496 |
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autosomal dominant tubulointerstitial kidney disease due to mutations in UMOD
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C4551496 |
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Nephropathy, familial, with gout
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C4551496 |
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UMOD-related autosomal dominant tubulointerstitial kidney disease
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C4551496 |
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UMOD familial juvenile hyperuricemic nephropathy
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C4551496 |
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UMOD-associated familial juvenile hyperuricemic nephropathy
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C4551496 |
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