Overview
Familial hemiplegic migraine type 2 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.
Difficulty finding words
Always present (100%)HP:0002381
Hemiparesis
Always present (100%)HP:0001269
Migraine headache
Always present (100%)HP:0002076
Nausea
Always present (100%)HP:0002018
Confusion
Very frequent (80-99%)HP:0001289
Brain swelling
Frequent (30-79%)HP:0002181
Generalized tonic-clonic seizure (without specification of onset)
Frequent (30-79%)HP:0002069
Migraine with aura
Frequent (30-79%)HP:0002077
Pyrexia
Frequent (30-79%)HP:0001945
Trance
Frequent (30-79%)HP:0001259
Abnormal finger-nose-finger test
Occasional (5-29%)HP:0001310
Inability to coordinate movements when walking
Occasional (5-29%)HP:0002066
Infratentorial atrophy
Occasional (5-29%)HP:0001272
Involuntary, rapid, rhythmic eye movements
Occasional (5-29%)HP:0000639
Localized motor seizures
Occasional (5-29%)HP:0011153
Tremor
Occasional (5-29%)HP:0001337
Apraxia
HP:0002186
Blurred vision
HP:0000622
Difficulty articulating speech
HP:0001260
Double vision
HP:0000651
Hemianopic blurring
HP:0001125
Nonprogressive mental retardation
Excluded (<1%)HP:0001249
Paralysis on one side of body
HP:0002301
Paroxysmal ataxia
HP:0002131
Sleepy
HP:0002329
Vertigo
HP:0002321
Related Conditions
Quick Facts
- SNOMED CT
- 1260330000
- UMLS CUI
- C1865322
- Fully Specified Name
- Familial hemiplegic migraine type 2 (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 26
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.