Term info
- OMIM:166700 (Orphanet:1306/e)
- DOID:0111536 (MONDO:equivalentTo)
- Orphanet:1306 (OMIM:166700)
- GARD:0001044 (MONDO:equivalentTo)
- MESH:C537415 (Orphanet:1306/e)
ordo_malformation_syndrome
https://github.com/monarch-initiative/mondo/issues/4521, https://github.com/monarch-initiative/mondo/issues/4948, https://github.com/monarch-initiative/mondo/issues/5682
Buschke-Ollendorff syndrome (BOS) is a benign disorder characterized by the association of osteopoikilosis lesions (``spotted bones'') in the skeleton and connective tissue nevi in the skin.
https://omim.org/entry/166700, http://identifiers.org/mesh/C537415, http://purl.obolibrary.org/obo/Orphanet_1306, http://purl.obolibrary.org/obo/DOID_0111536
http://purl.obolibrary.org/obo/MONDO_0019292, http://purl.obolibrary.org/obo/MONDO_0017198
Buschke-Ollendorff syndrome, disseminated dermatofibrosis with osteopoikilosis, osteopoikilosis with or without melorheostosis
osteopoikilosis, isolated, Buschke Ollendorff syndrome, osteopoikilosis with melorheostosis, Bos, dermatofibrosis, disseminated, with osteopoikilosis, Dermatoosteopoikilosis, dermatofibrosis, disseminated with osteopoikilosis, dermatofibrosis lenticularis disseminata with osteopoikilosis, osteopathia condensans disseminata, dermatofibrosis lenticularis disseminata, isolated
MONDO:0008157