Signs & Symptoms
Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.
Headache
Very frequent (80-99%)HP:0002315
Intracranial hypertension
Very frequent (80-99%)HP:0002516
Allergy
Frequent (30-79%)HP:0012393
Obesity
Frequent (30-79%)HP:0001513
Abnormal emotion processing
Occasional (5-29%)HP:0100851
Blurred vision
Occasional (5-29%)HP:0000622
Double vision
Occasional (5-29%)HP:0000651
Nausea
Occasional (5-29%)HP:0002018
Photophobia
Occasional (5-29%)HP:0000613
Scintillating scotoma
Occasional (5-29%)HP:0010822
Trouble sleeping
Occasional (5-29%)HP:0002360
Visual loss
Occasional (5-29%)HP:0000572
Vomiting
Occasional (5-29%)HP:0002013
Back pain
Very rare (1-4%)HP:0003418
Depression
Very rare (1-4%)HP:0000716
Dullness
Very rare (1-4%)HP:0001254
Focal olfactory seizure
Very rare (1-4%)HP:0011161
Migraine headache
Very rare (1-4%)HP:0002076
Pulsatile tinnitus
Very rare (1-4%)HP:0008629
Vertigo
Very rare (1-4%)HP:0002321
High blood pressure
HP:0000822
Papillitis
HP:0001085
Related Conditions
Pseudotumour cerebri due to drug(child)
Pseudotumour cerebri due to hypervitaminosis A(child)
Benign intracranial hypertension due to obesity(child)
Benign intracranial hypertension due to anaemia(child)
Benign intracranial hypertension due to metabolic disease(child)
Benign intracranial hypertension due to thrombus of intracranial vein(child)
Benign intracranial hypertension due to endocrine disease(child)
Encephalopathy(parent)
Quick Facts
- SNOMED CT
- 68267002
- UMLS CUI
- C0033845
- Fully Specified Name
- Benign intracranial hypertension (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 22
Medical Disclaimer
This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.
Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.