Overview
Congenital miosis 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 pupillary light reflex
Very frequent (80-99%)HP:0007695
Hypoplastic iris stroma
Very frequent (80-99%)HP:0007990
Iris hypopigmentation
Very frequent (80-99%)HP:0007730
Iris transillumination defect
Very frequent (80-99%)HP:0012805
Abnormal curving of the cornea or lens of the eye
Frequent (30-79%)HP:0000483
Axial myopia
Frequent (30-79%)HP:0031730
Elevated IOP
Frequent (30-79%)HP:0007906
Hemeralopia
Frequent (30-79%)HP:0012047
Nuclear cataract
Frequent (30-79%)HP:0100018
Photophobia
Frequent (30-79%)HP:0000613
Poor vision
Frequent (30-79%)HP:0000505
Primary open angle glaucoma
Frequent (30-79%)HP:0012108
Blindness
Occasional (5-29%)HP:0000618
Blurred vision
Occasional (5-29%)HP:0000622
Congenital cataracts, bilateral
Occasional (5-29%)HP:0000519
Corneal stromal edema
Occasional (5-29%)HP:0012040
Difficulties with night vision
Occasional (5-29%)HP:0000662
Glaucoma
Occasional (5-29%)HP:0000501
Increased corneal diameter
Occasional (5-29%)HP:0000485
Microcoria
HP:0025492
Miosis
HP:0000616
Near sighted
HP:0000545
Underdeveloped pupil dilator muscle
HP:0008345
Quick Facts
- SNOMED CT
- 400962005
- UMLS CUI
- C1303009
- Fully Specified Name
- Congenital miosis (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 23
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.