OBO ID: DOID:0080513
Term Name: Meier-Gorlin syndrome 2 Search Ontology:
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)
OTHER Meier-Gorlin syndrome 2 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
ORC4 Meier-Gorlin syndrome 2 613800
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None