About   Help   FAQ
Disease Ontology Browser
nonsyndromic aplasia cutis congenita (DOID:0080661)
Alliance: disease page
Synonyms: nonsyndromic aplasia cutis congenita
Alt IDs: OMIM:107600
Definition: A skin disease characterized by localized areas of missing skin that resemble ulcers or oopen wounds in new borns and that has_material_basis_in heterozygous mutation in the BMS1 gene on chromosome 10q11.

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)
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
MGI 6.15
The Jackson Laboratory