Disease Browser
Parent Node: Joint Diseases (D007592) ..Starting node .. Chondromatosis, Synovial (D015838) Child Nodes:
........Synovial Chondromatosis, Familial, with Dwarfism (C566087) 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: 2143
Name: Chondromatosis, Synovial
Definition: Rare, benign, chronic, progressive metaplasia in which cartilage is formed in the synovial membranes of joints, tendon sheaths, or bursae. Some of the metaplastic foci can become detached producing loose bodies. When the loose bodies undergo secondary calcification, the condition is called synovial osteochondromatosis.
Alternative IDs:
ParentIDs: MESH:D007592
TreeNumbers: C05.550.287
Synonyms: Chondromatoses, Synovial |Chondrometaplasias, Synovial |Chondrometaplasia, Synovial |Henderson Jones Syndrome |Henderson-Jones Syndrome |Osteochondromatoses, Synovial |Osteochondromatosis, Synovial |Reichel's Syndrome |Reichels Syndrome |Reichel Syndrome |Syndrome
Slim Mappings: Musculoskeletal disease
Reference:
MedGen: D015838
MeSH: D015838
OMIM: Genes: Phenotypes Disease Causing ClinVar Variants