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Human Disease

Meier-Gorlin syndrome 2

Term ID
DOID:0080513
Synonyms
Definition
A Meier-Gorlin syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the ORC4 gene on chromosome 2q23. https://www.omim.org/entry/613800
References
Ontology
Human Disease   ( DOID:0080513 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models