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Summary Literature (0)
OMIM:615008 - NEPHROTIC SYNDROME, TYPE 7; NPHS7


Xenbase Genes: dgke

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014005 - immunoglobulin-mediated membranoproliferative glomerulonephritis
MONDO:0016244 - atypical hemolytic-uremic syndrome
MONDO:0018159 - atypical hemolytic-uremic syndrome with DGKE deficiency
MONDO:0018904 - primary membranoproliferative glomerulonephritis

Disease Ontology (DO):
DOID:1184 - nephrotic syndrome