Overview
Haemochromatosis type 4A 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.
Increased ferritin
Frequent (30-79%)HP:0003281
Abnormal heart rate
Occasional (5-29%)HP:0011675
Cirrhosis
Occasional (5-29%)HP:0001394
Diabetes mellitus
Occasional (5-29%)HP:0000819
Elevated transferrin saturation
Occasional (5-29%)HP:0012463
Enlarged liver
Occasional (5-29%)HP:0002240
Fatty liver
Occasional (5-29%)HP:0001397
Melanoderma
Occasional (5-29%)HP:0000953
Osteoarthritis
Occasional (5-29%)HP:0002758
Tiredness
Occasional (5-29%)HP:0012378
Abnormal glucose tolerance
HP:0001952
Arthralgias
HP:0002829
Difficulty getting an erection
HP:0000802
Disease of the heart muscle
HP:0001638
Glucose tolerance decreased
HP:0040270
Lens opacities
HP:0000518
Low number of red blood cells or haemoglobin
HP:0001903
Quick Facts
- SNOMED CT
- 1303911001
- UMLS CUI
- C1853733
- Fully Specified Name
- Ferroportin disease (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 17
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.