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Summary Literature (1)
MIM:228930 - FIBULAR APLASIA OR HYPOPLASIA, FEMORAL BOWING, AND POLY-, SYN-, AND OLIGODACTYLY

Xenbase Genes: wnt7a

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0009232 - Fuhrmann syndrome

Disease Ontology (DO):
DOID:0090067 - Fuhrmann syndrome