Overview
Congenital analbuminemia 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.
Hypoalbuminaemia
Very frequent (80-99%)HP:0003073
Water retention
Very frequent (80-99%)HP:0000969
Birth weight less than 10th percentile
Frequent (30-79%)HP:0001518
Elevated serum cholesterol
Frequent (30-79%)HP:0003124
Hyperglobulinemia
Frequent (30-79%)HP:0010702
Hyperlipidemia
Frequent (30-79%)HP:0003077
Hypoproteinemia
Frequent (30-79%)HP:0003075
Inability to make and keep healthy fat tissue
Frequent (30-79%)HP:0009125
Increased alpha-globulin
Frequent (30-79%)HP:0005413
Leg edema
Frequent (30-79%)HP:0010741
Premature birth
Frequent (30-79%)HP:0001622
Tiredness
Frequent (30-79%)HP:0012378
Chronic lung infections
Occasional (5-29%)HP:0002783
Decreased amniotic fluid index
Occasional (5-29%)HP:0001562
Facial swelling
Occasional (5-29%)HP:0000282
Global developmental delay, mild
Occasional (5-29%)HP:0011342
Low pulse pressure
Occasional (5-29%)HP:0030851
Obesity
Occasional (5-29%)HP:0001513
Quick Facts
- SNOMED CT
- 718721006
- UMLS CUI
- C4305253
- Fully Specified Name
- Congenital analbuminemia (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 18
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.