MCKD2 gene

Known as: ADMCKD2, MCKD2, medullary cystic kidney disease 2 (autosomal dominant) 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1999-2009
02419992009

Papers overview

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2005
2005
BACKGROUND Autosomal-dominant juvenile hyperuricemia, gouty arthritis, medullary cysts, and progressive renal insufficiency are… (More)
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Highly Cited
2003
Highly Cited
2003
Familial juvenile hyperuricemic nephropathy (FJHN [MIM 162000]) is an autosomal-dominant disorder characterized by abnormal… (More)
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2003
2003
Medullary cystic kidney disease (MCKD) belongs with nephronophthisis (NPH) to the NPH-MCKD complex, a group of inherited… (More)
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2003
2003
BACKGROUND Autosomal dominant medullary cystic kidney disease (ADMCKD) is an inherited, distinct, chronic, tubulointerstitial… (More)
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Review
2003
Review
2003
Medullary cystic kidney disease (MCKD) belongs with nephronophthisis (NPH) in a group of inherited tubulo-interstitial nephritis… (More)
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2001
2001
BACKGROUND Autosomal-dominant medullary cystic kidney disease (MCKD) is an interstitial nephropathy characterized by structural… (More)
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2001
2001
BACKGROUND Autosomal-dominant medullary cystic kidney disease (ADMCKD) is characterized by the development of cysts at the… (More)
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2001
2001
BACKGROUND The location of a second genetic locus for autosomal dominant medullary cystic kidney disease (ADMCKD) at chromosome… (More)
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2000
2000
BACKGROUND Autosomal dominant medullary cystic kidney disease is a genetically heterogeneous nephropathy with clinical and… (More)
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1999
1999
Autosomal dominant medullary cystic disease (ADMCKD) is an interstitial nephropathy that has morphologic and clinical features… (More)
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