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.
Major histocompatibility complex class II deficiency
Congenital microvillous atrophy
Frequent (30-79%)
Pearson's syndrome
Occasional (5-29%)
Carbohydrate-deficient glycoprotein syndrome type I
Frequent (30-79%)
Netherton's syndrome
Congenital disorder of glycosylation type Ia
Frequent (30-79%)
Tricho-hepato-enteric syndrome
Frequent (30-79%)
Congenital tufting enteropathy
Very frequent (80-99%)
Asparagine-linked glycosylation 3 congenital disorder of glycosylation
Asparagine-linked glycosylation 9 congenital disorder of glycosylation
Occasional (5-29%)
X-linked immune dysregulation, polyendocrinopathy, enteropathy syndrome
Frequent (30-79%)
Refractory celiac disease
Always present (100%)
Combined immunodeficiency due to LRBA deficiency
Frequent (30-79%)
Periodic fever, infantile enterocolitis, autoinflammatory syndrome
Congenital disorder of glycosylation type 1b
Always present (100%)
Quick Facts
- SNOMED CT
- 275403002
- UMLS CUI
- C0554101
- Fully Specified Name
- Villous atrophy (finding)
- Associated Conditions
- 15
- 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.