Overview
Chondrocalcinosis is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Signs & Symptoms
Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.
Abnormality of the intervertebral disc
Very frequent (80-99%)HP:0005108
Arthralgias
Very frequent (80-99%)HP:0002829
Calcification of cartilage
Very frequent (80-99%)HP:0100593
Joint inflammation
Very frequent (80-99%)HP:0001369
Joint swelling
Very frequent (80-99%)HP:0001386
Osteoarthritis
Frequent (30-79%)HP:0002758
Ankylosis
Occasional (5-29%)HP:0031013
Calcium deposits in joints
Occasional (5-29%)HP:0000934
Decreased BMI
Occasional (5-29%)HP:0045082
Decreased bone mineral density Z score
Occasional (5-29%)HP:0004349
Increased inflammatory response
Occasional (5-29%)HP:0012649
Joint dislocation
Occasional (5-29%)HP:0001373
Limitation of joint mobility
Occasional (5-29%)HP:0001376
Pyrexia
Occasional (5-29%)HP:0001945
Stiff joint
Occasional (5-29%)HP:0001387
Synovitis
Occasional (5-29%)HP:0100769
Seizures
Very rare (1-4%)HP:0001250
Related Conditions
Idiopathic chondrocalcinosis(child)
Familial chondrocalcinosis(child)
Secondary chondrocalcinosis(child)
Hydroxyapatite arthropathy(child)
Intervertebral disk calcification(child)
Chondrocalcinosis of hand(child)
Chondrocalcinosis of joint of shoulder region(child)
Chondrocalcinosis of elbow joint(child)
Chondrocalcinosis of ankle AND/OR foot(child)
Chondrocalcinosis of knee joint(child)
Chondrocalcinosis of hip joint(child)
Chondrocalcinosis of wrist joint(child)
Chondrocalcinosis due to pyrophosphate crystals(child)
Chondrocalcinosis of joint of pelvis(child)
Calcification of laryngeal cartilage(child)
Keutel syndrome(child)
Spondyloepimetaphyseal dysplasia, short limb, abnormal calcification syndrome(child)
Chondrocalcinosis caused by dicalcium phosphate crystals(child)
Degenerative disorder of cartilage(parent)
Calcinosis(parent)
Quick Facts
- SNOMED CT
- 239838005
- UMLS CUI
- C0553730
- Fully Specified Name
- Chondrocalcinosis (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 17
Medical Disclaimer
This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.
Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.