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.
Osteogenesis imperfecta, dominant perinatal lethal
Always present (100%)
Hallermann-Streiff syndrome
Metaphyseal chondrodysplasia, Jansen type
Occasional (5-29%)
Ehlers-Danlos syndrome, hydroxylysine-deficient
Always present (100%)
Lethal multiple pterygium syndrome
Camptomelic dysplasia
Osteogenesis imperfecta
Very frequent (80-99%)
Osteogenesis imperfecta, perinatal lethal
Always present (100%)
Neonatal pseudo-hydrocephalic progeroid syndrome
Multiple symmetrical lipomatosis
Stuve-Wiedemann dysplasia
Osteogenesis imperfecta type IIA
Always present (100%)
Osteogenesis imperfecta type III
Transient neonatal hyperparathyroidism
Occasional (5-29%)
Lethal tight skin contracture syndrome
Very frequent (80-99%)
Pena-Shokeir syndrome type I
3-M syndrome
Frequent (30-79%)
Fryns syndrome
Microtia, absent patellae, micrognathia syndrome
Autosomal dominant centronuclear myopathy
Frequent (30-79%)
Shprintzen Goldberg craniosynostosis syndrome
X-linked dominant chondrodysplasia Chassaing Lacombe type
Frequent (30-79%)
Renal dysplasia with limb defect syndrome
Frequent (30-79%)
Van den Ende-Gupta syndrome
Frequent (30-79%)
Acrorenal mandibular syndrome
Frequent (30-79%)
Quick Facts
- SNOMED CT
- 249697003
- UMLS CUI
- C0426818
- Fully Specified Name
- Thin rib (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.