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Metadata
ID DOID:0080516
Name Meier-Gorlin syndrome 5
Definition A Meier-Gorlin syndrome that has_material_basis_in homozygous mutation in the CDC6 gene on chromosome 17q21.
https://www.omim.org/entry/613805
Xrefs

OMIM:613805

Parent Relationships

is_a Meier-Gorlin syndrome

is_a autosomal recessive disease

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