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.
Hereditary fructosuria
Glossopharyngeal neuralgia
Occasional (5-29%)
Recessive dystrophic epidermolysis bullosa
Hypertrophic gastritis
Frequent (30-79%)
Cleft palate with cleft lip
Occasional (5-29%)
Congenital junctional epidermolysis bullosa
Frequent (30-79%)
Wolman's disease
Frequent (30-79%)
Shwachman syndrome
Frequent (30-79%)
Glucose-galactose malabsorption
Frequent (30-79%)
Congenital microvillous atrophy
AA amyloidosis
Frequent (30-79%)
Lysinuric protein intolerance
Netherton's syndrome
Always present (100%)
Marchiafava-Bignami disease
Very frequent (80-99%)
Junctional epidermolysis bullosa gravis of Herlitz
Frequent (30-79%)
Hypertrophic gastropathy
Frequent (30-79%)
Pellagra
Frequent (30-79%)
Chylomicron retention disease
Idiopathic achalasia of esophagus
Occasional (5-29%)
Tropical endomyocardial fibrosis
Frequent (30-79%)
LAL (Lysosomal acid lipase) deficiency
Occasional (5-29%)
Chronic hiccup
Frequent (30-79%)
Mitochondrial neurogastrointestinal encephalomyopathy syndrome
Oculogastrointestinal muscular dystrophy
Pancreatic insufficiency, dyserythropoietic anemia, calvarial hyperostosis syndrome
Quick Facts
- SNOMED CT
- 248325000
- UMLS CUI
- C0162429
- Fully Specified Name
- Undernourished (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.