OBO ID: DOID:0080515
Term Name: Meier-Gorlin syndrome 4 Search Ontology:
Synonyms:
Definition: A Meier-Gorlin syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the CDT1 gene on chromosome 16q24. https://www.omim.org/entry/613804
References:
Ontology: Human Disease   (DOID:0080515)
OTHER Meier-Gorlin syndrome 4 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
CDT1 Meier-Gorlin syndrome 4 613804
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None