Overview
Coxoauricular 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.
Abnormality of pelvic girdle bone morphology
Very frequent (80-99%)HP:0002644
Abnormality of the thighbone
Very frequent (80-99%)HP:0002823
Deafness
Very frequent (80-99%)HP:0000365
Decreased body height
Very frequent (80-99%)HP:0004322
Decreased bone mineral density Z score
Very frequent (80-99%)HP:0004349
Dislocated femoral heads
Very frequent (80-99%)HP:0002827
External auditory meatal atresia
Very frequent (80-99%)HP:0000413
Micromelia
Very frequent (80-99%)HP:0002983
Microtia
Very frequent (80-99%)HP:0008551
Related Conditions
Microtia(parent)
Multiple system malformation syndrome(parent)
Hearing loss associated with syndrome(parent)
Small stature(parent)
Hereditary disorder of musculoskeletal system(parent)
Congenital anomaly of skeletal bone(parent)
Congenital anomaly of ear with impairment of hearing(parent)
Skeletal dysplasia(parent)
Hip pathological dislocation(parent)
Developmental hereditary disorder(parent)
Injury of external ear(parent)
BI - Bone injury(parent)
Hereditary hearing loss(parent)
Quick Facts
- SNOMED CT
- 732248005
- UMLS CUI
- C1852513
- Fully Specified Name
- Coxoauricular syndrome (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 9
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.