Overview
Braddock syndrome is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Signs & Symptoms
Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.
Glottic web
Very frequent (80-99%)HP:0005950
Grey sclerae
Very frequent (80-99%)HP:0000592
Hemivertebra
Very frequent (80-99%)HP:0002937
Intrauterine growth retardation, IUGR
Very frequent (80-99%)HP:0001511
Missing ribs
Very frequent (80-99%)HP:0000921
Overfolded helix
Very frequent (80-99%)HP:0000396
Pectus excavatum
Very frequent (80-99%)HP:0000767
Posteriorly angulated ears
Very frequent (80-99%)HP:0000358
Pulmonary artery hypertension
Very frequent (80-99%)HP:0002092
Pulmonary fibrosis
Very frequent (80-99%)HP:0002206
Abnormal distribution of hair
Frequent (30-79%)HP:0010720
Blepharophimosis
Frequent (30-79%)HP:0000581
Decreased body height
Frequent (30-79%)HP:0004322
Decreased projection of lower jaw
Frequent (30-79%)HP:0000347
Ocular hypotelorism
Frequent (30-79%)HP:0000601
Palpebronasal fold
Frequent (30-79%)HP:0000286
Postnatal failure to thrive
Frequent (30-79%)HP:0001508
Preaxial hand polydactyly
Frequent (30-79%)HP:0001177
Respiratory distress, neonatal
Frequent (30-79%)HP:0002643
Scoliosis
Frequent (30-79%)HP:0002650
Short neck
Frequent (30-79%)HP:0000470
Single kidney
Frequent (30-79%)HP:0000122
Torticollis, congenital
Frequent (30-79%)HP:0005988
Wide-spaced nipples
Frequent (30-79%)HP:0006610
Quick Facts
- SNOMED CT
- 720575002
- UMLS CUI
- C4303988
- Fully Specified Name
- Braddock syndrome (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 24
Medical Disclaimer
This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.
Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.