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Summary Literature (0)
MIM:615721 - RENAL HYPODYSPLASIA/APLASIA 2; RHDA2

Xenbase Genes: fgf20

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014319 - renal hypodysplasia/aplasia 2
MONDO:0018470 - renal agenesis