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.
Glucagonoma syndrome
Occasional (5-29%)
Glycogenosis with glucoaminophosphaturia
Frequent (30-79%)
Infantile nephropathic cystinosis
Frequent (30-79%)
Johanson-Blizzard syndrome
Always present (100%)
Sickle cell anemia
Occasional (5-29%)
Cystinosis
Frequent (30-79%)
Fumarase deficiency
Always present (100%)
3-Beta-hydroxy-delta-5-C27-steroid dehydrogenase deficiency
Delta-4-3-oxosteroid-5-beta-reductase deficiency
Vasoactive intestinal peptide-secreting tumour
Occasional (5-29%)
Delta cell tumor
Occasional (5-29%)
Pancreatic polypeptidoma
Occasional (5-29%)
Sickling disorder due to hemoglobin S
Occasional (5-29%)
Low phospholipid associated cholelithiasis
Very frequent (80-99%)
Neonatal intrahepatic cholestasis due to citrin deficiency
Caroli disease
Frequent (30-79%)
Lathosterolosis
Frequent (30-79%)
Intellectual disability, enteropathy, deafness, peripheral neuropathy, ichthyosis, keratoderma syndrome
Frequent (30-79%)
PGM1-related congenital disorder of glycosylation
Occasional (5-29%)
Navajo neuropathy
Always present (100%)
Progressive familial intrahepatic cholestasis type 2
Progressive familial intrahepatic cholestasis type 3
Caroli syndrome
Very frequent (80-99%)
PFIC4 - progressive familial intrahepatic cholestasis type 4
Always present (100%)
Quick Facts
- SNOMED CT
- 4637005
- UMLS CUI
- C0008372
- Fully Specified Name
- Intrahepatic cholestasis (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.