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.
Argininosuccinate lyase deficiency
Cryptococcosis
Very rare (1-4%)
Japanese encephalitis virus disease
Occasional (5-29%)
Hemiplegic migraine
Frequent (30-79%)
Reye's syndrome
Ornithine carbamoyltransferase deficiency
Acute disseminated encephalomyelitis
Frequent (30-79%)
Merosin deficient congenital muscular dystrophy
Frequent (30-79%)
Deficiency of citrulline-aspartate ligase
MCAD deficiency
Acute liver failure
Occasional (5-29%)
Fulminant hepatic failure
Occasional (5-29%)
Nicotinamide adenine dinucleotide coenzyme Q reductase deficiency
Free-living amoeba infection
Occasional (5-29%)
Glioblastoma multiforme
Frequent (30-79%)
Citrullinaemia
Ethylene glycol poisoning
Very rare (1-4%)
Herpes encephalitis
Occasional (5-29%)
Reversible cerebral vasoconstriction syndrome
Very rare (1-4%)
Snyder-Robinson syndrome
Very rare (1-4%)
Congenital malformation of dural sinus
Very rare (1-4%)
Hemorrhagic fever caused by Lujo virus
Occasional (5-29%)
Citrullinemia type II
Occasional (5-29%)
Familial acute necrotizing encephalopathy
Frequent (30-79%)
Acyl-CoA dehydrogenase 9 deficiency
Occasional (5-29%)
Quick Facts
- SNOMED CT
- 85974009
- UMLS CUI
- C0270614
- Fully Specified Name
- Mass of intracranial structure (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.