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Summary Literature (0)
MIM:614326 - FEINGOLD SYNDROME 2; FGLDS2

Xenbase Genes:

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013691 - Feingold syndrome type 2
MONDO:0015267 - Feingold syndrome

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