About   Help   FAQ
Disease Ontology Browser
Meckel syndrome 6 (DOID:0070120)
Alliance: disease page
Synonyms: Meckel-Gruber syndrome, type 6; MKS6
Alt IDs: OMIM:612284, ICD10CM:Q61.9
Definition: A Meckel syndrome that has_material_basis_in an autosomal recessive mutation of the CC2D2A gene on chromosome 4p15.32.

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support. 		last database update
04/09/2024
MGI 6.23 		The Jackson Laboratory