Visualize Submit Comment

Metadata
ID	DOID:0080515
Name	Meier-Gorlin syndrome 4
Definition	A Meier-Gorlin syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the CDT1 gene on chromosome 16q24. https://www.omim.org/entry/613804
Xrefs	OMIM:613804
Parent Relationships	is_a Meier-Gorlin syndrome is_a autosomal recessive disease