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ID	DOID:0061295
PURL	http://purl.obolibrary.org/obo/DOID_0061295 Copy Copied!
Name	Meckel syndrome 10
Definition	A Meckel syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the B9D2 gene on chromosome 19q13. https://pubmed.ncbi.nlm.nih.gov/31411728/
Xrefs	MIM:614175
Parent Relationships	is_a Meckel syndrome is_a autosomal recessive disease
Subclass Logical Relationships	has material basis in some autosomal recessive inheritance