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CLDN16

claudin 16

gene with protein productOMIM: 6039591 заболевание
GeneCards ↗Open Targets ↗NCBI Gene ↗OMIM ↗

Ассоциированные заболевания

Disease-causing germline mutation(s) (loss of function) in1
Primary hypomagnesemia with hypercalciuria and nephrocalcinosis without severe ocular involvementORPHA:31043
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Данные: Orphadata (CC-BY-4.0)