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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)
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Send questions and comments to User Support. 		last database update
11/12/2024
MGI 6.24 		The Jackson Laboratory