FTH1-associated iron overload

disorder

SNOMED 1230310007CUI C1851316

Overview

FTH1-associated iron overload 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.

Elevated hepatic iron concentration

Always present (100%)HP:0012465

Elevated transferrin saturation

Always present (100%)HP:0012463

Increased circulating iron concentration

Always present (100%)HP:0003452

Increased ferritin

Always present (100%)HP:0003281

Abnormal circulating ceruloplasmin concentration

Excluded (<1%)HP:0033144

Abnormal circulating copper concentration

Excluded (<1%)HP:0010836

Abnormal circulating transferrin concentration

Excluded (<1%)HP:0032385

Decreased haemoglobin

Excluded (<1%)HP:0001903

Related Conditions

Autosomal dominant hereditary disorder(parent)

Metabolic and genetic disorder affecting the liver(parent)

Hereditary hemochromatosis(parent)

Digestive system hereditary disorder(parent)

Quick Facts

SNOMED CT: 1230310007
UMLS CUI: C1851316
Fully Specified Name: Ferritin heavy chain 1-related iron overload (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 8

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.