Overview
Clinical overview and emergency guidance are pending physician authorship. Graph-derived data (ontology codes, linked conditions, diagnostic biomarkers) is available below.
Associated Conditions
Conditions associated with this symptom based on HPO disease-phenotype annotations.
Neonatal hemochromatosis
Very frequent (80-99%)
Congenital dyserythropoietic anemia, type III
Frequent (30-79%)
Hereditary hemochromatosis
Juvenile hemochromatosis
Always present (100%)
Porphyria cutanea tarda
Frequent (30-79%)
Deficiency of phosphoenolpyruvate kinase
Frequent (30-79%)
Idiopathic haemochromatosis
Primary haemochromatosis
Growth retardation, amino aciduria, cholestasis, iron overload, lactic acidosis, and early death
Tricho-hepato-enteric syndrome
Hemochromatosis type 3
Severe congenital hypochromic anemia with ringed sideroblasts
Frequent (30-79%)
Cerebro-cutaneous syndrome with iron overload
Always present (100%)
Haemochromatosis type 1
FTH1-associated iron overload
Always present (100%)
Quick Facts
- SNOMED CT
- 165624002
- UMLS CUI
- C0151900
- Fully Specified Name
- Serum iron above reference range (finding)
- Associated Conditions
- 15
- Diagnostic Tests
- 0
This information is for educational purposes only. If you are experiencing symptoms, please consult a healthcare provider for proper evaluation and diagnosis.