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.
Neonatal hemochromatosis
Insulin receptor defect
Arginase deficiency
Always present (100%)
Polycystic kidney disease, infantile type
Frequent (30-79%)
alpha-1-Proteinase inhibitor deficiency
Occasional (5-29%)
Arteriohepatic dysplasia
Very frequent (80-99%)
Shigellosis
Very rare (1-4%)
Polyostotic fibrous dysplasia of bone
Very rare (1-4%)
Cutis laxa, x-linked
Frequent (30-79%)
Familial visceral amyloidosis, Ostertag type
Progressive intrahepatic cholestasis
Very frequent (80-99%)
Congenital biliary atresia
Very frequent (80-99%)
Isolated corticotropin deficiency
Leprechaunism syndrome
Infection by Shigella
Very rare (1-4%)
Deficiency of heptulokinase
Frequent (30-79%)
Primary sclerosing cholangitis
Very frequent (80-99%)
Familial atrial myxoma
Occasional (5-29%)
Glycogen phosphorylase kinase deficiency
Occasional (5-29%)
Secondary hypoadrenalism
Mitochondrial trifunctional protein deficiency
Occasional (5-29%)
Delta-4-3-oxosteroid-5-beta-reductase deficiency
Frequent (30-79%)
Bifunctional peroxisomal enzyme deficiency
Occasional (5-29%)
Saldino-Mainzer dysplasia
Occasional (5-29%)
AA amyloidosis
Frequent (30-79%)
Quick Facts
- SNOMED CT
- 33688009
- UMLS CUI
- C0008370
- Fully Specified Name
- Cholestasis (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.