Meier-Gorlin syndrome 4

Term ID

DOID:0080515

Synonyms

Definition

A Meier-Gorlin syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the CDT1 gene on chromosome 16q24. https://pubmed.ncbi.nlm.nih.gov/21358631/

References

• MIM:613804

Ontology

Human Disease   ( DOID:0080515 )