Disease Browser
Parent Node: Joint Diseases (D007592) ..Starting node .. Joint Loose Bodies (D007594) Child Nodes:
Sister Nodes: ..Ankylosis (D000844) 10 ..Arthralgia (D018771) 1 ..Arthritis (D001168) 57 ..Arthrogryposis (D001176) 55 ..Arthropathy, Neurogenic (D001177) 3 ..Borrone Di Rocco Crovato syndrome (C536577) ..Brachydactylous dwarfism Mseleni type (C537086) ..Bursitis (D002062) 1 ..Calcification of Joints and Arteries (C565891) ..Chondromatosis, Synovial (D015838) 1 ..Contracture (D003286) 41 ..Coracoclavicular Joint, Anomalous (C565161) ..Cushing's symphalangism (C536223) ..Dwarfism stiff joint ocular abnormalities (C535724) ..Femoracetabular Impingement (D057925) ..Flynn Aird syndrome (C537066) ..GEMSS syndrome (C537679) ..Growth mental deficiency syndrome of Myhre (C537620) ..Hallux Limitus (D020857) ..Hallux Rigidus (D020859) ..Hemarthrosis (D006395) ..Hip Dysplasia, Beukes Type (C564185) ..Hydrarthrosis (D006833) ..Joint Deformities, Acquired (D016916) ..Joint Instability (D007593) 17 ..Joint Loose Bodies (D007594) ..Laplane Fontaine Lagardere syndrome (C537869) ..Laryngotracheal Stenosis, Progressive, with Short Stature and Arthropathy (C566379) ..Leri pleonosteosis (C537118) ..Metatarsalgia (D037061) ..Morillo-Cucci Passarge syndrome (C536983) ..Nail-Patella Syndrome (D009261) 1 ..Osteoarthropathy, Primary Hypertrophic (D010004) 2 ..Osteoarthropathy, Secondary Hypertrophic (D010005) ..Patellofemoral Pain Syndrome (D046788) ..Pfeiffer Palm Teller syndrome (C537889) ..Short stature and locking fingers (C537603) ..Shoulder Impingement Syndrome (D019534) ..Synovitis (D013585) 5 ..Temporomandibular Joint Disorders (D013705) 2 ..Thai Symphalangism Syndrome (C564303) Human Disease MESH is developed by UMLS . Further data from MedGen , OMIM , CTD
Term ID: 5976
Name: Joint Loose Bodies
Definition: Fibrous, bony, cartilaginous and osteocartilaginous fragments in a synovial joint. Major causes are osteochondritis dissecans, synovial chondromatosis, osteophytes, fractured articular surfaces and damaged menisci.
Alternative IDs:
ParentIDs: MESH:D007592
TreeNumbers: C05.550.535
Synonyms: Joint Loose Body |Loose Bodies, Joint |Loose Body, Joint
Slim Mappings: Musculoskeletal disease
Reference:
MedGen: D007594
MeSH: D007594
OMIM: Genes: Phenotypes Disease Causing ClinVar Variants