OBO ID: DOID:0080514
Term Name: Meier-Gorlin syndrome 3 Search Ontology:
Synonyms:
Definition: A Meier-Gorlin syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the ORC6 gene on chromosome 16q11. https://www.omim.org/entry/613803
References:
Ontology: Human Disease   (DOID:0080514)
OTHER Meier-Gorlin syndrome 3 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
ORC6 Meier-Gorlin syndrome 3 613803
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None