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Diseases

Familial Hemiplegic Migraine

familial hemiplegic migraine

Entity Type
Diseases
Relation Groups
1
Relation Preview
8

Basic Information

Grouped by core information, identifiers, and descriptions.

Quick relations do not expand inferred candidates by default. Load path-derived ingredients or herbs when needed.

Core Information

Disease Name
Familial Hemiplegic Migraine
Standard Disease Name
familial hemiplegic migraine
MeSH Tree
No data
ICD-10
No data

Identifiers

DO ID
No data
MeSH ID
D020325
OMIM ID
No data
UMLS ID
C0338484
HPO ID
No data

Description and Extensions

Description
NCI2016_NICHD_1602D:A migraine disorder characterized by individual and family history of aura that includes motor weakness.|NCI2016_02D:A migraine disorder characterized by individual and family history of aura that includes motor weakness.
Related

Direct relations and traceable candidates grouped by relation type.

Related Targets

target disease8 Targets
01
ATP1A2
ATPase Na+/K+ transporting subunit alpha 2
ATPase Na+/K+ transporting subunit alpha 2
02
ATP1A4
ATPase Na+/K+ transporting subunit alpha 4
ATPase Na+/K+ transporting subunit alpha 4
03
CACNA1C
calcium voltage-gated channel subunit alpha1 C
calcium voltage-gated channel subunit alpha1 C
04
CALCA
calcitonin related polypeptide alpha
calcitonin related polypeptide alpha
05
IL1RN
interleukin 1 receptor antagonist
interleukin 1 receptor antagonist
07
SCN1A
sodium voltage-gated channel alpha subunit 1
sodium voltage-gated channel alpha subunit 1