loading...| Preferred Name |
Osteochondritis dissecans |
| ID |
http://www.orpha.net/ORDO/Orphanet_2764 |
| alternative_term |
König disease |
| definition |
Osteochondritis dissecans (OCD) is a rare bone disease characterized by an acquired idiopathic necrotic lesion of subchondral bone with the formation of a sequestrum, which may detach to form loose bodies in joints. OCD mainly affects the knee, ankle and elbow joints and can lead to pain, functional limitations and secondary osteoarthritis. |
| definition_citation |
Orphanet |
| expertlink |
https://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2764 |
| has_age_of_onset |
All ages |
| has_inheritance |
Not applicable |
| hasDbXref |
ICD-10:M93.2 MeSH:D010008 UMLS:C0029421 MedDRA:10031231 ICD-11:FB82.1 |
| label |
Osteochondritis dissecans |
| notation |
ORPHA:2764 |
| part_of | |
| prefixIRI |
ORDO:Orphanet_2764 |
| prefLabel |
Osteochondritis dissecans |
| present_in |
Europe AND has_point_prevalence_average_value : 35.0 AND has_point_prevalence_range : 1-5 / 10 000 |
| treeView | |
| subClassOf |