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MIM:613702 - KLIPPEL-FEIL SYNDROME 3, AUTOSOMAL DOMINANT; KFS3
Xenbase Genes: gdf3
Human Disease Resource: OMIM
MONDO:0013375 - Klippel-Feil syndrome 3, autosomal dominant |
MONDO:0016520 - isolated Klippel-Feil syndrome |
DOID:10426 - Klippel-Feil syndrome |