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References | OMIM | Gene | GeneReviews | HGMD | HGNC |
GENATLAS PHENOTYPE |
last update : 16-09-2015 |
Symbol | NPHP13 |
Location | 4p14 |
Name | nephronophthisis 13 |
Corresponding gene | WDR19 |
Main clinical features |
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Genetic determination | autosomal recessive |
Function/system disorder | kidney and urinary tract |
Type | disease |
Remark(s) |