OBO ID: DOID:0080512
Term Name: Meier-Gorlin syndrome 1 Search Ontology:
Synonyms:
Definition: A Meier-Gorlin syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the ORC1 gene on chromosome 1p32. https://www.omim.org/entry/224690
References:
Ontology: Human Disease   (DOID:0080512)
OTHER Meier-Gorlin syndrome 1 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
ORC1 Meier-Gorlin syndrome 1 224690
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None