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ID	DOID:0061297
PURL	http://purl.obolibrary.org/obo/DOID_0061297 Copy Copied!
Name	Meckel syndrome 12
Definition	A Meckel syndrome that has_material_basis_in a compound heterozygous mutation in the KIF14 gene on chromosome 1q31. https://pubmed.ncbi.nlm.nih.gov/24128419/
Xrefs	MIM:616258
Parent Relationships	is_a Meckel syndrome is_a autosomal recessive disease
Subclass Logical Relationships	has material basis in some autosomal recessive inheritance