Home Contact Sitemap

PedAM

Pediatric Disease Annotations & Medicines




Disease nephrocalcinosis
Phenotype C0015624|fanconi syndrome
Sentences 1
PubMedID- 24285859 In conclusion, we present a novel atypical cause of autosomal-dominant fanconi syndrome with nephrocalcinosis caused by the hnf4a r76w mutation.

Page: 1