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.
Primary intestinal lymphangiectasia
Frequent (30-79%)
Juvenile polyposis syndrome
Very rare (1-4%)
Dengue
Occasional (5-29%)
Intestinal enteropeptidase deficiency
Hypertrophic gastritis
Frequent (30-79%)
Johanson-Blizzard syndrome
Frequent (30-79%)
Chediak-Higashi syndrome
Occasional (5-29%)
Deficiency of enterokinase
Finnish congenital nephrotic syndrome
Always present (100%)
Very long chain acyl-CoA dehydrogenase deficiency
Very rare (1-4%)
Connective tissue disease overlap syndrome
Occasional (5-29%)
Mixed collagen vascular disease
Occasional (5-29%)
Familial haemophagocytic lymphohistiocytosis
Hypertrophic gastropathy
Frequent (30-79%)
Citrullinemia type II
Frequent (30-79%)
Congenital analbuminemia
Frequent (30-79%)
Aplasia cutis congenita with intestinal lymphangiectasia syndrome
Frequent (30-79%)
Severe combined immunodeficiency with hypereosinophilia
Pierson syndrome
Congenital disorder of glycosylation type 1j
Occasional (5-29%)
Deafness, small bowel diverticulosis, neuropathy syndrome
Refractory celiac disease
Frequent (30-79%)
PGBM1 - polyglucosan body myopathy type 1
Frequent (30-79%)
CHAPLE (complement hyperactivation, angiopathic thrombosis, protein losing enteropathy) syndrome
Quick Facts
- SNOMED CT
- 166778002
- UMLS CUI
- C0392692
- Fully Specified Name
- Serum proteins below reference range (finding)
- Associated Conditions
- 24
- 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.