OBO ID: DOID:0080518
Term Name: Meier-Gorlin syndrome 7 Search Ontology:
Synonyms:
Definition: A Meier-Gorlin syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the CDC45 gene on chromosome 22q11. https://www.omim.org/entry/617063
References:
Ontology: Human Disease   (DOID:0080518)
OTHER Meier-Gorlin syndrome 7 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
CDC45 Meier-Gorlin syndrome 7 617063
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None