Meckel syndrome 2 Disease Ontology Browser

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Disease Ontology Browser

Meckel syndrome 2 (DOID:0070116)
Alliance: disease page
Synonyms: Meckel-Gruber syndrome, type 2; MKS2
Alt IDs: OMIM:603194, ICD10CM:Q61.9
Definition: A Meckel syndrome that has_material_basis_in an autosomal recessive mutation of the TMEM216 gene on chromosome 11q12.2.

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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