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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 the TCTN2 gene 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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04/16/2024
MGI 6.23 		The Jackson Laboratory