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Disease Ontology Browser
Meckel syndrome 3 (DOID:0070117)
Alliance: disease page
Synonyms: Meckel-Gruber syndrome, type 3; MKS3
Alt IDs: OMIM:607361, ICD10CM:Q61.9
Definition: A Meckel syndrome that has_material_basis_in an autosomal recessive mutation of TMEM67 on chromosome 8q22.1.

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
MGI 6.14
The Jackson Laboratory