Overview
Lattice corneal dystrophy 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.
Amyloid cardiomyopathy
Always present (100%)HP:0030843
End-stage renal disease
Always present (100%)HP:0003774
Nephrosis
Always present (100%)HP:0000100
Renal glomerular amyloid deposition
Always present (100%)HP:0032614
Decrease in blood pressure upon standing up
Frequent (30-79%)HP:0001278
Lattice corneal dystrophy
Frequent (30-79%)HP:0001149
Loose skin
Frequent (30-79%)HP:0000973
Cataract
Occasional (5-29%)HP:0000518
Damaged optic nerve
Occasional (5-29%)HP:0001138
Disease of the heart muscle
Occasional (5-29%)HP:0001638
Urolithiasis
Occasional (5-29%)HP:0034368
Bulbar muscle weakness
HP:0001283
Generalised amyloid deposition
HP:0003216
Polyneuropathy
HP:0001271
Reduced heart rate variability
HP:0031861
Renal failure
HP:0000083
Related Conditions
Lattice corneal dystrophy Type I(child)
Lattice corneal dystrophy of bilateral corneas(child)
Stromal corneal dystrophy(parent)
Connective tissue hereditary disorder(parent)
Hereditary corneal dystrophy(parent)
Autosomal dominant hereditary disorder(parent)
Organ limited hereditary amyloidosis(parent)
Amyloid of cornea(parent)
Quick Facts
- SNOMED CT
- 361199007
- UMLS CUI
- C0155127
- Fully Specified Name
- Lattice corneal dystrophy (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 16
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.