Migraine, Familial Hemiplegic, 2 (FHM2)

Alias:
Migraine, Familial Basilar
Fhm2
Mhp2
Familial Hemiplegic Migraine 2
Migraine, Hemiplegic, Familial, Type 2
Familial Hemiplegic Migraine-2
Familiar Basilar Migraine
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Migraine, Familial Hemiplegic, 2, also known as migraine, familial basilar, is related to headache and benign epilepsy with centrotemporal spikes, and has symptoms including fever, hemiparesis and hemiplegia. An important gene associated with Migraine, Familial Hemiplegic, 2 is ATP1A2 (ATPase Na+/K+ Transporting Subunit Alpha 2), and among its related pathways/superpathways are Cardiac conduction and Neuropathic Pain-Signaling in Dorsal Horn Neurons. Affiliated tissues include brain and smooth muscle, and related phenotypes are aphasia and migraine
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Unknown
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22
214
26

Medical Symptom

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Categorization
Description
HPO Frequency
Orphanet Frequency
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No data available

Gene & Mutation

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No data available

Disease Model

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Name
MGI
Related Gene
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Publications
No data available

References Literature

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