Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (0)
DOID:0111536 - Buschke-Ollendorff syndrome


Disease Ontology Definition:A syndrome characterized by multiple subcutaneous nevi or nodules and osteopoikilosis that has_material_basis_in heterozygous mutation in the LEMD3 gene on chromosome 12q14.3.

Synonyms: BOS, dermatofibrosis lenticularis disseminata with osteopoikilosis, dermatoosteopoikilosis, disseminated dermatofibrosis with osteopoikilosis, osteopathia condensans disseminata,

Xenbase Genes : lemd3



Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal dominant disease (is_a), syndrome (is_a)