Overview
Familial hemiplegic migraine type 1 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.
Intermittent migraine headaches
Always present (100%)HP:0002076
Seizures
Occasional (5-29%)HP:0001250
Tremor
Occasional (5-29%)HP:0001337
Acalculia
HP:0002442
Agitation
HP:0000713
Ataxia
HP:0001251
Atrophic cerebellum
HP:0001272
Confusion
HP:0001289
Difficulty finding words
HP:0002381
Excessive, persistent worry and fear
HP:0000739
Hearing sounds
HP:0008765
Hemianopic blurring
HP:0001125
Hemiparesis
HP:0001269
Involuntary, rapid, rhythmic eye movements
HP:0000639
Migraine with aura
HP:0002077
Paralysis on one side of body
HP:0002301
Psychosis
HP:0000709
Pyrexia
HP:0001945
Sleepy
HP:0002329
Stupor
HP:0001259
Visual hallucination
HP:0002367
Related Conditions
Quick Facts
- SNOMED CT
- 1260329005
- UMLS CUI
- C1832884
- Fully Specified Name
- Familial hemiplegic migraine type 1 (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 21
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.