Overview
Clinical overview and emergency guidance are pending physician authorship. Graph-derived data (ontology codes, linked conditions, diagnostic biomarkers) is available below.
Associated Conditions
Conditions associated with this symptom based on HPO disease-phenotype annotations.
Weill-Marchesani syndrome
Occasional (5-29%)
Caudal dysplasia sequence
Frequent (30-79%)
Osteopoikilosis
Mucopolysaccharidosis, MPS-III-D
Leri-Weill dyschondrosteosis
Very frequent (80-99%)
GM1 Gangliosidosis type II
Always present (100%)
Holt-Oram syndrome
Very frequent (80-99%)
Pseudoachondroplastic spondyloepiphyseal dysplasia syndrome
Occasional (5-29%)
Metatropic dysplasia group
Very frequent (80-99%)
Proteus syndrome
Occasional (5-29%)
Cystathionine beta-synthase deficiency
Frequent (30-79%)
Mucopolysaccharidosis, MPS-I-H/S
Always present (100%)
Juvenile osteochondrosis of second metatarsal
Frequent (30-79%)
Schwartz-Jampel syndrome
Very frequent (80-99%)
Thanatophoric dysplasia
Occasional (5-29%)
Nager syndrome
Frequent (30-79%)
Mietens syndrome
Very frequent (80-99%)
De Lange syndrome
Frequent (30-79%)
Cerebro-oculo-facio-skeletal syndrome
Very frequent (80-99%)
Mucopolysaccharidosis, MPS-III-A
Mucopolysaccharidosis, MPS-VII
Frequent (30-79%)
Melorheostosis
Very frequent (80-99%)
Paroxysmal choreoathetosis
Occasional (5-29%)
Werner syndrome
Occasional (5-29%)
Freeman-Sheldon syndrome
Very frequent (80-99%)
Quick Facts
- SNOMED CT
- 84445001
- UMLS CUI
- C0162298
- Fully Specified Name
- Joint stiffness (finding)
- Associated Conditions
- 25
- Diagnostic Tests
- 0
This information is for educational purposes only. If you are experiencing symptoms, please consult a healthcare provider for proper evaluation and diagnosis.