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.
Atrophia bulborum hereditaria
Occasional (5-29%)
Ehlers-Danlos syndrome, type 4
Occasional (5-29%)
Familial dysautonomia
Very frequent (80-99%)
Arteriohepatic dysplasia
Occasional (5-29%)
Charcot-Marie-Tooth disease, type IB
Frequent (30-79%)
Duane's syndrome
Occasional (5-29%)
Lens-induced iridocyclitis
Frequent (30-79%)
9p partial trisomy syndrome
Very frequent (80-99%)
X-linked ocular albinism, Nettleship type
Very frequent (80-99%)
Lowe syndrome
Very frequent (80-99%)
Myopathy with tubular aggregates
Occasional (5-29%)
Lens-induced uveitis
Frequent (30-79%)
X-linked corneal dermoid
Frequent (30-79%)
Charcot-Marie-Tooth disease and deafness
Frequent (30-79%)
Proteus like syndrome
Very frequent (80-99%)
Hydrocephalus with endocardial fibroelastosis and cataract syndrome
Frequent (30-79%)
Hirschsprung disease, ganglioneuroblastoma syndrome
Very frequent (80-99%)
Triopia
Very frequent (80-99%)
Quick Facts
- SNOMED CT
- 274093008
- UMLS CUI
- C0154936
- Fully Specified Name
- Abnormal pupil (finding)
- Associated Conditions
- 18
- 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.