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Summary Literature (0)
MIM:613702 - KLIPPEL-FEIL SYNDROME 3, AUTOSOMAL DOMINANT; KFS3

Xenbase Genes: gdf3

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013375 - Klippel-Feil syndrome 3, autosomal dominant
MONDO:0016520 - obsolete isolated Klippel-Feil syndrome

Disease Ontology (DO):
DOID:10426 - Klippel-Feil syndrome