Overview
Russell Weaver Bull 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.
Abnormal gastrointestinal tract morphology
Very frequent (80-99%)HP:0012718
Abnormal morphology of female internal genitalia
Very frequent (80-99%)HP:0000008
Abnormal spinal segmentation
Very frequent (80-99%)HP:0003422
Abnormal vertebral bodies
Very frequent (80-99%)HP:0003312
Abnormality of pelvic girdle bone morphology
Very frequent (80-99%)HP:0002644
Abnormality of the intestine
Very frequent (80-99%)HP:0002242
Abnormality of the knee
Very frequent (80-99%)HP:0002815
Abnormality of the liver
Very frequent (80-99%)HP:0001392
Abnormality of the reproductive system
Very frequent (80-99%)HP:0000078
Abnormality of the spleen
Very frequent (80-99%)HP:0001743
Abnormality of the ureter
Very frequent (80-99%)HP:0000069
Abnormality of the urinary system
Very frequent (80-99%)HP:0000079
Absent/small lungs
Very frequent (80-99%)HP:0006703
Anal atresia
Very frequent (80-99%)HP:0002023
Anorectal anomaly
Very frequent (80-99%)HP:0012732
Cerebral cortex atrophy
Very frequent (80-99%)HP:0002120
Decreased body height
Very frequent (80-99%)HP:0004322
Decreased projection of mandible
Very frequent (80-99%)HP:0000347
Diaphragmatic hernia
Very frequent (80-99%)HP:0000776
Epibulbar dermoid
Very frequent (80-99%)HP:0001140
Gastro-esophageal reflux
Very frequent (80-99%)HP:0002020
Gum enlargement
Very frequent (80-99%)HP:0000212
Increased distance between eyes
Very frequent (80-99%)HP:0000316
Microtia
Very frequent (80-99%)HP:0008551
Missing ribs
Very frequent (80-99%)HP:0000921
Nonsyndromal hydrocephalus
Very frequent (80-99%)HP:0000238
Oligohydramnios
Very frequent (80-99%)HP:0001562
Omphalocoele
Very frequent (80-99%)HP:0001539
Preauricular skin tags
Very frequent (80-99%)HP:0000384
Premature birth
Very frequent (80-99%)HP:0001622
Related Conditions
Quick Facts
- SNOMED CT
- 765755006
- UMLS CUI
- C2931613
- Fully Specified Name
- Axial mesodermal dysplasia spectrum (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 30
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.