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Metadata
ID	DOID:0080590
Name	Klippel-Feil syndrome 2
Definition	A Klippel-Feil syndrome that has_material_basis_in homozygous mutation in the MEOX1 gene on chromosome 17q21. https://www.ncbi.nlm.nih.gov/pubmed/23290072
Xrefs	MIM:214300
Parent Relationships	is_a Klippel-Feil syndrome is_a autosomal recessive disease
Subclass Logical Relationships	has material basis in some autosomal recessive inheritance