medullary cystic kidney disease
(Q1916694)
inherited form of cystic kidney disease leading to fibrosis and impaired renal function that is caused by mutations in the UMOD gene, which encodes uromodulin/Tamm-Horsfall mucoprotein
inherited form of cystic kidney disease leading to fibrosis and impaired renal function that is caused by mutations in the UMOD gene, which encodes uromodulin/Tamm-Horsfall mucoprotein
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Current Data About
medullary cystic kidney disease
| (P31) |
(Q929833)
(Q112193867) |
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| (P279) |
(Q1425737)
(Q12136) |
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| (P1748) |
C123172
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| (P1995) |
(Q1071953)
|
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| (P2293) |
(Q14905564)
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| (P2888) |
http://www.orpha.net/ORDO/Orphanet_34149
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other details
| aliases |
MEDULLARY CYSTIC KIDNEY DISEASE 2; MCKD2 Medullary Cystic Kidney Disease type 2 MCKD2 Medullary Cystic Kidney Disease 2, Autosomal Dominant MEDULLARY CYSTIC KIDNEY DISEASE 2 Medullary Cystic Kidney Disease Type II |
| description | inherited form of cystic kidney disease leading to fibrosis and impaired renal function that is caused by mutations in the UMOD gene, which encodes uromodulin/Tamm-Horsfall mucoprotein |
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