Meckel syndrome 11 Disease Ontology Browser

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Disease Ontology Browser

Meckel syndrome 11 (DOID:0061296)
Alliance: disease page
Alt IDs: OMIM:615397
Definition: A Meckel syndrome that has_material_basis_in homozygous mutation in the TMEM231 gene on chromosome 16q23.

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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