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Metadata
ID	DOID:0080591
Name	Klippel-Feil syndrome 3
Definition	A Klippel-Feil syndrome that has_material_basis_in heterozygous mutation in the GDF3 gene on chromosome 12p13. https://www.ncbi.nlm.nih.gov/pubmed/19864492
Xrefs	MIM:613702
Parent Relationships	is_a autosomal dominant disease is_a Klippel-Feil syndrome
Subclass Logical Relationships	has material basis in some autosomal dominant inheritance