Signs & Symptoms
Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.
Abnormal cell morphology
Very frequent (80-99%)HP:0025461
Abnormal nervous system physiology
Frequent (30-79%)HP:0012638
Cerebral oedema
Frequent (30-79%)HP:0002181
Corpus callosum abnormality
Frequent (30-79%)HP:0001273
Cortical white matter abnormalities seen on MRI
Frequent (30-79%)HP:0002500
Emotional lability
Frequent (30-79%)HP:0000712
Headache
Frequent (30-79%)HP:0002315
Language impairment
Frequent (30-79%)HP:0002463
Muscle weakness
Frequent (30-79%)HP:0001324
Paralysis
Frequent (30-79%)HP:0003470
Tiredness
Frequent (30-79%)HP:0012378
Visual loss
Frequent (30-79%)HP:0000572
Epilepsy
Occasional (5-29%)HP:0001250
Memory impairment
Occasional (5-29%)HP:0002354
Astrocytoma
HP:0009592
Ependymoma
HP:0002888
Glioblastoma
HP:0012174
Quick Facts
- SNOMED CT
- 393563007
- UMLS CUI
- C1621958
- Fully Specified Name
- Glioblastoma multiforme (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 17
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.