Overview
Congenital atransferrinemia 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.
Decreased haemoglobin
Very frequent (80-99%)HP:0001903
Susceptibility to infection
Frequent (30-79%)HP:0002719
Abnormality of the cardiovascular system
Occasional (5-29%)HP:0001626
Abnormality of the pancreas
Occasional (5-29%)HP:0001732
Arthritis
Occasional (5-29%)HP:0001369
Hypothyroidism
Occasional (5-29%)HP:0000821
Atransferrinemia
HP:0012239
Chronic heart failure
HP:0001635
Hypochromic anemia
HP:0001931
Liver disease
HP:0001392
Related Conditions
Quick Facts
- SNOMED CT
- 111571009
- UMLS CUI
- C0521802
- Fully Specified Name
- Congenital atransferrinemia (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 10
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.