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Disease Ontology Browser
Adams-Oliver syndrome 4 (DOID:0061346)
Alliance: disease page
Synonyms: AOS4
Alt IDs: OMIM:615297
Definition: An Adams-Oliver syndrome that is characterized by aplasia cutis congenita and terminal transverse limb defects. Additional abnormalities may be present in other organs, e.g., heart, brain, and/or eyes and that has_material_basis_in homozygous mutation in the EOGT gene on chromosome 3p14.1.

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