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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 LEMD3 on chromosome 12q14.3.

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

Xenbase Genes : lemd3


OMIM:
OMIM:166700 - BUSCHKE-OLLENDORFF SYNDROME; BOS

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)