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Gene Expression Ontology
Last uploaded:
December 16, 2015
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| Preferred Name | Migraine, familial hemiplegic, 1 | |
| Synonyms |
FHM1 |
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| Definitions |
(FHM1) - A subtype of migraine with aura associated with ictal hemiparesis and, in some families, cerebellar ataxia and atrophy. 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. |
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| ID |
http://identifiers.org/omim/141500 |
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| altLabel |
FHM1
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| definition |
(FHM1) - A subtype of migraine with aura associated with ictal hemiparesis and, in some families, cerebellar ataxia and atrophy. 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.
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| id |
OMIM:141500
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| notation |
OMIM:141500
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| prefLabel |
Migraine, familial hemiplegic, 1
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| subClassOf |
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