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Disease Ontology Browser
Adams-Oliver syndrome 2 (DOID:0061345)
Alliance: disease page
Synonyms: AOS2
Alt IDs: OMIM:614219
Definition: An Adams-Oliver syndrome that is characterized by aplasia cutis congenita and terminal transverse limb defects, in association with variable involvement of the brain, eyes, and cardiovascular systems and that has_material_basis_in homozygous or compound heterozygous mutation in the DOCK6 gene on chromosome 19p13.2.

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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Send questions and comments to User Support. 		last database update
09/08/2026
MGI 6.24 		The Jackson Laboratory