OBO ID: DOID:0080516
Term Name: Meier-Gorlin syndrome 5 Search Ontology:
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)
OTHER Meier-Gorlin syndrome 5 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
CDC6 ?Meier-Gorlin syndrome 5 613805
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None