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.
Caudal dysplasia sequence
Occasional (5-29%)
Femoral hypoplasia - unusual facies syndrome
Poland anomaly
Occasional (5-29%)
Robinow syndrome
Occasional (5-29%)
Aicardi's syndrome
Frequent (30-79%)
Multiple lentigines syndrome
Deficiency of phosphoribosylaminoimidazole carboxylase
Frequent (30-79%)
Kyphomelic dysplasia
Frequent (30-79%)
Delleman-Oorthuys syndrome
Occasional (5-29%)
AEG - anophthalmia-esophageal-genital syndrome
Distal partial deletion of long arm of chromosome 11
Frequent (30-79%)
Isochromosome 9p
Occasional (5-29%)
Autosomal dominant spondylocostal dysostosis
Occasional (5-29%)
Steinfeld syndrome
Occasional (5-29%)
Tetraamelia with multiple malformation syndrome
Frequent (30-79%)
Craniocerebellocardiac dysplasia
Occasional (5-29%)
Shprintzen Goldberg craniosynostosis syndrome
Occasional (5-29%)
Acrorenal mandibular syndrome
Braddock syndrome
Very frequent (80-99%)
Aural atresia with multiple congenital anomalies and intellectual disability syndrome
Frequent (30-79%)
Diaphanospondylodysostosis
Spondylocostal dysostosis with anal atresia and genitourinary malformation syndrome
Thoraco-abdominal enteric duplication
Very frequent (80-99%)
Russell Weaver Bull syndrome
Very frequent (80-99%)
Imperforate oropharynx, costovertebral anomalies syndrome
Very frequent (80-99%)
Quick Facts
- SNOMED CT
- 249695006
- UMLS CUI
- C0426816
- Fully Specified Name
- Absence of 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.