hydrolethalus syndrome 2 Disease Ontology Browser

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Disease Ontology Browser

hydrolethalus syndrome 2 (DOID:0111356)
Alliance: disease page
Synonyms: HLS2
Alt IDs: OMIM:614120
Definition: A hydrolethalus syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the KIF7 gene on chromosome 15q26.1.

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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