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migraine, familial hemiplegic, 2

Disease Summary
Associated Targets (1)
Tclin

1


Mondo Description Any familial or sporadic hemiplegic migraine in which the cause of the disease is a mutation in the ATP1A2 gene.
Uniprot Description A subtype of migraine with aura associated with hemiparesis in some families. Migraine is a disabling symptom complex of periodic headaches, usually temporal and unilateral. Headaches are often accompanied by irritability, nausea, vomiting and photophobia, preceded by constriction of the cranial arteries. Migraine with aura is characterized by recurrent attacks of reversible neurological symptoms (aura) that precede or accompany the headache. Aura may include a combination of sensory disturbances, such as blurred vision, hallucinations, vertigo, numbness and difficulty in concentrating and speaking.
Mondo Term and Equivalent IDs
MONDO:0011232:  migraine, familial hemiplegic, 2
DOID:0111182: 
GARD:0010095: 
UMLS:C1865322: