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Disease Ontology Browser
Meckel syndrome 8 (DOID:0070122)
Alliance: disease page
Synonyms: Meckel-Gruber syndrome, type 8; MKS8
Alt IDs: OMIM:613885, ICD10CM:Q61.9, ORDO:90674
Definition: A Meckel syndrome that has_material_basis_in an autosomal recessive mutation of TCTN2 on chromosome 12q24.31.


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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last database update
01/12/2022
MGI 6.17
The Jackson Laboratory