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.
Phosphoenolpyruvate carboxykinase (GTP) deficiency
Occasional (5-29%)
Glycogen storage disease, type IV
Very frequent (80-99%)
Echinococcus multilocularis infection
Frequent (30-79%)
Glutaric aciduria, type 2
Occasional (5-29%)
Dihydrolipoamide dehydrogenase deficiency
Occasional (5-29%)
Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome
Frequent (30-79%)
Sarcoidosis
Frequent (30-79%)
Niemann-Pick disease, type B
Frequent (30-79%)
Erythropoietic protoporphyria
Occasional (5-29%)
Familial visceral amyloidosis, Ostertag type
Occasional (5-29%)
Cytochrome-c oxidase deficiency
Reye's syndrome
Frequent (30-79%)
Congenital biliary atresia
Frequent (30-79%)
Chediak-Higashi syndrome
Frequent (30-79%)
Deficiency of glycerone-transferase
Deficiency of branching enzyme
Very frequent (80-99%)
Deficiency of uridyl transferase
Deficiency of maleylacetoacetate isomerase
Excluded (<1%)
MCAD deficiency
Frequent (30-79%)
Beta thalassemia intermedia
Occasional (5-29%)
Patent ductus venosus
Methotrexate poisoning
Frequent (30-79%)
3-Methylglutaconic aciduria type 4
Occasional (5-29%)
Aggressive lymphadenopathic mastocytosis with eosinophilia
Occasional (5-29%)
Familial haemophagocytic lymphohistiocytosis
Frequent (30-79%)
Related Symptoms
Quick Facts
- SNOMED CT
- 77981007
- UMLS CUI
- C0232744
- Fully Specified Name
- Decreased liver function (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.