Signs & Symptoms
Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.
Defective or absent horizontal voluntary eye movements
Very frequent (80-99%)HP:0000657
Duane anomaly
Very frequent (80-99%)HP:0009921
Eye movement issue
Very frequent (80-99%)HP:0000496
Oculomotor neuropathy
Very frequent (80-99%)HP:0012246
Short palpebral fissure
Very frequent (80-99%)HP:0012745
Squint
Very frequent (80-99%)HP:0000486
Abnormal vertebral segmentation and fusion
Frequent (30-79%)HP:0005640
Blepharophimosis
Frequent (30-79%)HP:0000581
Enophthalmos
Frequent (30-79%)HP:0000490
Impaired ocular abduction
Frequent (30-79%)HP:0000634
Impaired ocular adduction
Frequent (30-79%)HP:0000542
Low posterior hair line
Frequent (30-79%)HP:0002162
Nostrils anteverted
Frequent (30-79%)HP:0000463
Sensorineural deafness
Frequent (30-79%)HP:0000407
Abnormal pupil morphology
Occasional (5-29%)HP:0000615
Abnormal vertebral bodies
Occasional (5-29%)HP:0003312
Abnormality of cardiovascular system morphology
Occasional (5-29%)HP:0030680
absence of radius and ulna
Occasional (5-29%)HP:0003974
Aniridia
Occasional (5-29%)HP:0000526
Anorectal anomaly
Occasional (5-29%)HP:0012732
Aplastic/hypoplastic thumbs
Occasional (5-29%)HP:0009601
Brachydactyly
Occasional (5-29%)HP:0001156
Broad flat nasal bridge
Occasional (5-29%)HP:0000431
Camptodactyly
Occasional (5-29%)HP:0012385
Cleft of palate
Occasional (5-29%)HP:0000175
Coloboma of choroid
Occasional (5-29%)HP:0000567
Compensatory head posture
Occasional (5-29%)HP:0031705
Decreased corneal diameter
Occasional (5-29%)HP:0000482
Decreased size of cranium
Occasional (5-29%)HP:0000252
Dysplastic ears
Occasional (5-29%)HP:0000377
Related Conditions
Duane's syndrome, type 1(child)
Duane's syndrome, type 2(child)
Duane's syndrome, type 3(child)
Duane syndrome with vertical deviation(child)
Okihiro syndrome(child)
Duane's syndrome of right eye(child)
Duane's syndrome of left eye(child)
Wildervanck's syndrome(child)
Congenital strabismus(parent)
Congenital anomaly of peripheral nerve(parent)
Abducens nerve disorder(parent)
Congenital anomaly of eye(parent)
Congenital anomaly of nervous system of head/neck(parent)
Quick Facts
- SNOMED CT
- 60318001
- UMLS CUI
- C0013261
- Fully Specified Name
- Duane's syndrome (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.