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.
Biliary cirrhosis
Occasional (5-29%)
Primary intestinal lymphangiectasia
Frequent (30-79%)
Juvenile polyposis syndrome
Glycogen storage disease, type IV
Frequent (30-79%)
Toxic shock syndrome
Occasional (5-29%)
AL amyloidosis
Occasional (5-29%)
Primary biliary cirrhosis
Occasional (5-29%)
Smith-Lemli-Opitz syndrome
Always present (100%)
Hypertrophic gastritis
Frequent (30-79%)
Histiocytosis X
Occasional (5-29%)
Acute febrile mucocutaneous lymph node syndrome
Frequent (30-79%)
Marburg virus disease
Occasional (5-29%)
Mesangiocapillary glomerulonephritis
Occasional (5-29%)
Leishmaniasis
Frequent (30-79%)
Wilson's disease
Always present (100%)
Deficiency of branching enzyme
Frequent (30-79%)
ABL - Abetalipoproteinaemia
Frequent (30-79%)
Westphal-Strumpell syndrome
Always present (100%)
Primary sclerosing cholangitis
Occasional (5-29%)
Finnish congenital nephrotic syndrome
Always present (100%)
Hennekam lymphangiectasia-lymphoedema syndrome
Insulin resistance - type B
Frequent (30-79%)
Generalised pustular psoriasis
Occasional (5-29%)
Wolcott-Rallison dysplasia
Frequent (30-79%)
Dowling-Meara epidermolysis bullosa
Occasional (5-29%)
Quick Facts
- SNOMED CT
- 127355002
- UMLS CUI
- C0860864
- Fully Specified Name
- Albumin below reference range (finding)
- Associated Conditions
- 25
- 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.