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Metadata
ID	DOID:0080592
Name	Klippel-Feil syndrome 4
Definition	A Klippel-Feil syndrome that has_material_basis_in homozygous mutation in the MYO18B gene on chromosome 22q12. https://www.ncbi.nlm.nih.gov/pubmed/25748484
Xrefs	MIM:616549 ORDO:447974
Subsets	DO_rare_slim
Parent Relationships	is_a Klippel-Feil syndrome is_a autosomal recessive disease
Subclass Logical Relationships	has material basis in some autosomal recessive inheritance