Search Ontology:
Human Disease

Meier-Gorlin syndrome 5

Term ID
DOID:0080516
Synonyms
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
References
Ontology
Human Disease   ( DOID:0080516 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
Citations
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