Signs & Symptoms
Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.
Abdominal discomfort
HP:0002027
Abnormal glucose tolerance
HP:0001952
Abnormal heart rate
HP:0011675
Abnormal liver function tests
HP:0002910
Amenorrhea
HP:0000141
Ascites
HP:0001541
Azoospermia
HP:0000027
Chronic heart failure
HP:0001635
Cirrhosis
HP:0001394
Diabetes mellitus
HP:0000819
Difficulty getting an erection
HP:0000802
Disease of the heart muscle
HP:0001638
Disease of the joints
HP:0003040
Enlarged liver
HP:0002240
Fluid around lungs
HP:0002202
Hair loss
HP:0001596
Hepatocellular carcinoma
HP:0001402
Hyperferritinemia
HP:0003281
Increased circulating iron concentration
HP:0003452
Increased heart size
HP:0001640
Large spleen
HP:0001744
Low gonadotropins (secondary hypogonadism)
HP:0000044
Osteoporosis
HP:0000939
Patchy darkened skin
HP:0000953
Telangiectasia
HP:0001009
Testicular degeneration
HP:0000029
Related Conditions
Hemochromatosis type 3(child)
Hemochromatosis type 4(child)
Juvenile hemochromatosis(child)
Haemochromatosis type 1(child)
FTH1-associated iron overload(child)
Digenic haemochromatosis(child)
SLC40A1-related haemochromatosis(child)
Haemochromatosis type 4A(child)
Hemochromatosis(parent)
Hereditary metabolic disease(parent)
Quick Facts
- SNOMED CT
- 35400008
- UMLS CUI
- C0392514
- Fully Specified Name
- Hereditary 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.