Search Ontology:
Human Disease
Meier-Gorlin syndrome 6
- Term ID
- DOID:0080517
- Synonyms
-
- Definition
- A Meier-Gorlin syndrome that has_material_basis_in heterozygous mutation in the GMNN gene on chromosome 6p22. https://pubmed.ncbi.nlm.nih.gov/26637980/
- References
- Ontology
- Human Disease ( DOID:0080517 )
- is a type of
-
Show first 5 Terms
Other Pages
Genes Involved
Zebrafish Models