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.
Hallermann-Streiff syndrome
Very frequent (80-99%)
Achondrogenesis, type IB
Fibrochondrogenesis
Very frequent (80-99%)
Congenital hemidysplasia with ichthyosiform erythroderma and limb defects syndrome
Occasional (5-29%)
Metatropic dysplasia group
Very frequent (80-99%)
Metaphyseal chondrodysplasia, Jansen type
Poland anomaly
Occasional (5-29%)
Oto-palato-digital syndrome, type II
Achondrogenesis, type IA
Always present (100%)
Infantile hypophosphatasia
Chondroectodermal dysplasia
Weaver syndrome
Pseudo-Hurler polydystrophy
Cleidocranial dysostosis
Gorlin syndrome
Short rib-polydactyly syndrome, Majewski type
Jeune thoracic dystrophy
Achondroplasia
Always present (100%)
Lethal Kniest-like syndrome
Occasional (5-29%)
Rolland-Debuqois syndrome
Hypochondrogenesis
Focal dermal hypoplasia
Frequent (30-79%)
Schneckenbecken dysplasia
Very frequent (80-99%)
Type III short rib polydactyly syndrome
Very frequent (80-99%)
Beemer-Langer type short rib polydactyly syndrome
Quick Facts
- SNOMED CT
- 249696007
- UMLS CUI
- C0426817
- Fully Specified Name
- Short 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.