Search Ontology:
Human Disease
Meier-Gorlin syndrome 8
- Term ID
- DOID:0080255
- Synonyms
-
- Definition
- A Meier-Gorlin syndrome that has_material_basis_in compound heterozygous mutation in the MCM5 gene on chromosome 22q12. https://www.omim.org/entry/617564
- References
- Ontology
- Human Disease ( DOID:0080255 )
- is a type of
-
Show first 5 Terms
Other Pages
Genes Involved
Zebrafish Models
Citations