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.
Schinzel-Giedion syndrome
Atelosteogenesis
Always present (100%)
Escobar syndrome
Pachydermoperiostosis syndrome
Pachydermoperiostosis of nail
Osteodysplastic primordial dwarfism, type 1
Greenberg dysplasia
Always present (100%)
Pelvis shoulder dysplasia
Frequent (30-79%)
Pelviscapular dysplasia
Cranioosteoarthropathy
Agammaglobulinemia, microcephaly, craniosynostosis, severe dermatitis syndrome
Occasional (5-29%)
Atelosteogenesis type 1
Always present (100%)
Joubert syndrome with JATD (Jeune asphyxiating thoracic dystrophy)
Occasional (5-29%)
Kagami Ogata syndrome
Occasional (5-29%)
Paternal uniparental disomy of chromosome 14
Occasional (5-29%)
Majewski osteodysplastic primordial dwarfism type II
Occasional (5-29%)
Quick Facts
- SNOMED CT
- 249687007
- UMLS CUI
- C0426808
- Fully Specified Name
- Long clavicle (finding)
- Associated Conditions
- 16
- 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.