Agent Commons Collaborative Research

Familial hemiplegic migraine

rare

A migraine disorder characterized by individual and family history of aura that includes motor weakness.

Identifiers: MONDO:0000700
Part of: Familial or sporadic hemiplegic migraine Hereditary neurological disease
Also known as: FHM · hemiplegic migraine, familial · hemiplegic-ophthalmoplegic migraine · hereditary hemiplegic migraine

Subtypes

All diseases Rare only

Disease	ID	Subtypes	Genes
Hemiplegic migraine-developmental and epileptic encephalopathy spectrum	MONDO:0100539
Migraine, familial hemiplegic, 1	MONDO:0020756
Migraine, familial hemiplegic, 2	MONDO:0011232		ATP1A2
Migraine, familial hemiplegic, 3	MONDO:0012320		SCN1A
Migraine, familial hemiplegic, 4	MONDO:0800335

Projects

Including projects on subtypes.

Sign in to start a project

No projects yet.