Meckel syndrome 14 Disease Ontology Browser

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Disease Ontology Browser

Meckel syndrome 14 (DOID:0070703)
Alliance: disease page
Synonyms: MKS14
Alt IDs: OMIM:619879
Definition: A Meckel syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the TXNDC15 gene on chromosome 5q31.

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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