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Human Disease

Meier-Gorlin syndrome 8

Term ID
DOID:0080255
Synonyms
Definition
A Meier-Gorlin syndrome that has_material_basis_in compound heterozygous mutation in the MCM5 gene on chromosome 22q12. https://pubmed.ncbi.nlm.nih.gov/28198391/
References
Ontology
Human Disease   ( DOID:0080255 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models