Meier-Gorlin syndrome 7

Term ID

DOID:0080518

Synonyms

Definition

A Meier-Gorlin syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the CDC45 gene on chromosome 22q11. https://pubmed.ncbi.nlm.nih.gov/27374770/

References

• MIM:617063

Ontology

Human Disease   ( DOID:0080518 )