Diese bisher noch wenig charakterisierte Erkrankung ist durch eine rezidivierende Nephrolithiasis und begleitende chronmische Diarrhoe gekennzeichnet. Uasgelöst werden könnte sie durch Mutationen des SLC26A6-Gens.
Hereditäre Urolithiasis | ||||
Cystinurie | ||||
Dicarboxyl-Aminoazidurie | ||||
Dihydroxyadenin-Urolithiasis | ||||
Nephrocalcinose | ||||
Nephrolithiasis-Diarrhoe-Syndrom | ||||
SLC26A6 | ||||
Prädisposition zur Urolithiasis | ||||
Uratnephropathie | ||||
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OMIM.ORG article Omim 167030 |