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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

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)