Signs & Symptoms
Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.
Increased ferritin
Very frequent (80-99%)HP:0003281
Elevated hepatic iron concentration
Frequent (30-79%)HP:0012465
Elevated transferrin saturation
Frequent (30-79%)HP:0012463
Hepatic periportal necrosis
Frequent (30-79%)HP:0002614
Hepatitis
Frequent (30-79%)HP:0012115
Liver fibrosis
Frequent (30-79%)HP:0001395
Viral hepatitis
Frequent (30-79%)HP:0006562
Abnormal shape of thyroid gland
Occasional (5-29%)HP:0011772
Abnormality of adrenal morphology
Occasional (5-29%)HP:0011732
Abnormality of the reproductive system
Occasional (5-29%)HP:0000078
Abnormally shaped pancreas
Occasional (5-29%)HP:0012090
Cardiac anomaly
Occasional (5-29%)HP:0001627
Chronic infection
Occasional (5-29%)HP:0031035
Cushing syndrome
Occasional (5-29%)HP:0003118
Diabetes mellitus
Occasional (5-29%)HP:0000819
Enlarged liver
Occasional (5-29%)HP:0002240
Fatty liver
Occasional (5-29%)HP:0001397
Heart failure
Occasional (5-29%)HP:0001635
Hepatic bridging fibrosis
Occasional (5-29%)HP:0012852
Increased incidence of hepatocellular carcinoma
Occasional (5-29%)HP:0001402
Low levels of vitamin C
Occasional (5-29%)HP:0100510
Micronodular cirrhosis
Occasional (5-29%)HP:0001413
Esophageal carcinoma
Very rare (1-4%)HP:0011459
Osteoporosis
Very rare (1-4%)HP:0000939
Peritonitis
Very rare (1-4%)HP:0002586
Laboratory abnormality
HP:0001939
Related Conditions
Quick Facts
- SNOMED CT
- 66576001
- UMLS CUI
- C0268063
- Fully Specified Name
- African nutritional hemochromatosis (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 26
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.