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Summary Literature (0)
MIM:164280 - FEINGOLD SYNDROME 1; FGLDS1

Xenbase Genes: mycn

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0008115 - Feingold syndrome type 1
MONDO:0015267 - Feingold syndrome

Disease Ontology (DO):
DOID:0060464 - Feingold syndrome