Overview
Hereditary cavernous hemangioma of brain is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Signs & Symptoms
Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.
Cerebral cavernous malformation
Always present (100%)HP:0033522
Cerebral hemorrhage
Very frequent (80-99%)HP:0001342
Headache
Very frequent (80-99%)HP:0002315
Seizures
Very frequent (80-99%)HP:0001250
Cavernous haemangioma
Frequent (30-79%)HP:0001048
Focal T2 hyperintense brainstem lesion
Frequent (30-79%)HP:0012748
Focal T2 hypointense brainstem lesion
Frequent (30-79%)HP:0012749
Hemangiomata
Frequent (30-79%)HP:0001028
Hypoaesthesia
Frequent (30-79%)HP:0033748
Muscle weakness
Frequent (30-79%)HP:0001324
Paresthesia
Frequent (30-79%)HP:0003401
Pinched nerve
Frequent (30-79%)HP:0030430
Pseudotumor cerebri
Frequent (30-79%)HP:0002516
Scoliosis
Frequent (30-79%)HP:0002650
Choroidal hemangioma
Occasional (5-29%)HP:0007872
Frequent vomiting
Occasional (5-29%)HP:0002572
Intellectual impairment
Occasional (5-29%)HP:0100543
Retinal cavernous hemangioma
Occasional (5-29%)HP:0011513
Spinal cord lesion
Occasional (5-29%)HP:0100561
Vascular abnormalities restricted to skin
Occasional (5-29%)HP:0011276
Venous malformations
Occasional (5-29%)HP:0012721
Adrenal calcification
Very rare (1-4%)HP:0010512
Astrocytoma
Very rare (1-4%)HP:0009592
Meningioma
Very rare (1-4%)HP:0002858
Vestibular Schwann cell tumor
Very rare (1-4%)HP:0009588
Quick Facts
- SNOMED CT
- 717003001
- UMLS CUI
- C2931263
- Fully Specified Name
- Hereditary cavernous hemangioma of brain (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 25
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.