1260330000: Familial hemiplegic migraine type 2 (disorder)

SNOMED CT Concept\Clinical finding (finding)\...

\Head finding (finding)\Finding of brain\Disorder of brain (disorder)\Migraine with aura\Hemiplegic migraine\Familial hemiplegic migraine\Migraine type caused by mutations in the ATP1A2 gene.
\Head finding (finding)\Finding of head region\Hemiplegic migraine\Familial hemiplegic migraine\Migraine type caused by mutations in the ATP1A2 gene.
\Head finding (finding)\Disorder of head (disorder)\Headache disorder\Vascular headache\Migraine\Migraine with aura\Hemiplegic migraine\Familial hemiplegic migraine\Migraine type caused by mutations in the ATP1A2 gene.
\Head finding (finding)\Disorder of head (disorder)\Disorder of brain (disorder)\Migraine with aura\Hemiplegic migraine\Familial hemiplegic migraine\Migraine type caused by mutations in the ATP1A2 gene.
\Head finding (finding)\Headache\Headache disorder\Vascular headache\Migraine\Migraine with aura\Hemiplegic migraine\Familial hemiplegic migraine\Migraine type caused by mutations in the ATP1A2 gene.

\General finding of soft tissue\Blood vessel finding\Vascular disorder\Vascular headache\Migraine\Migraine with aura\Hemiplegic migraine\Familial hemiplegic migraine\Migraine type caused by mutations in the ATP1A2 gene.
\General finding of soft tissue\Disorder of soft tissue\Vascular disorder\Vascular headache\Migraine\Migraine with aura\Hemiplegic migraine\Familial hemiplegic migraine\Migraine type caused by mutations in the ATP1A2 gene.

\Central nervous system finding\Finding of brain\Disorder of brain (disorder)\Migraine with aura\Hemiplegic migraine\Familial hemiplegic migraine\Migraine type caused by mutations in the ATP1A2 gene.
\Central nervous system finding\Disorder of the central nervous system (disorder)\Disorder of brain (disorder)\Migraine with aura\Hemiplegic migraine\Familial hemiplegic migraine\Migraine type caused by mutations in the ATP1A2 gene.

\Cardiovascular finding\Pain of cardiovascular structure\Vascular headache\Migraine\Migraine with aura\Hemiplegic migraine\Familial hemiplegic migraine\Migraine type caused by mutations in the ATP1A2 gene.
\Cardiovascular finding\Disorder of cardiovascular system (disorder)\Cardiovascular system hereditary disorder\Familial hemiplegic migraine\Migraine type caused by mutations in the ATP1A2 gene.
\Cardiovascular finding\Disorder of cardiovascular system (disorder)\Vascular disorder\Vascular headache\Migraine\Migraine with aura\Hemiplegic migraine\Familial hemiplegic migraine\Migraine type caused by mutations in the ATP1A2 gene.
\Cardiovascular finding\Blood vessel finding\Vascular disorder\Vascular headache\Migraine\Migraine with aura\Hemiplegic migraine\Familial hemiplegic migraine\Migraine type caused by mutations in the ATP1A2 gene.

\Neurological finding\Sensory nervous system finding\...

\Finding of sensation by site (finding)\Pain finding at anatomical site\...

\Pain of cardiovascular structure\Vascular headache\Migraine\Migraine with aura\Hemiplegic migraine\Familial hemiplegic migraine\Migraine type caused by mutations in the ATP1A2 gene.

\Headache\Headache disorder\Vascular headache\Migraine\Migraine with aura\Hemiplegic migraine\Familial hemiplegic migraine\Migraine type caused by mutations in the ATP1A2 gene.

\Pain / sensation finding\Pain\Pain finding at anatomical site\...

\Pain of cardiovascular structure\Vascular headache\Migraine\Migraine with aura\Hemiplegic migraine\Familial hemiplegic migraine\Migraine type caused by mutations in the ATP1A2 gene.

\Headache\Headache disorder\Vascular headache\Migraine\Migraine with aura\Hemiplegic migraine\Familial hemiplegic migraine\Migraine type caused by mutations in the ATP1A2 gene.

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of nervous system\Familial hemiplegic migraine\Migraine type caused by mutations in the ATP1A2 gene.
\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Cardiovascular system hereditary disorder\Familial hemiplegic migraine\Migraine type caused by mutations in the ATP1A2 gene.
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder (disorder)\Familial hemiplegic migraine\Migraine type caused by mutations in the ATP1A2 gene.
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of nervous system\Familial hemiplegic migraine\Migraine type caused by mutations in the ATP1A2 gene.
\Disease\Disorder of body system\Hereditary disorder by system\Cardiovascular system hereditary disorder\Familial hemiplegic migraine\Migraine type caused by mutations in the ATP1A2 gene.
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Hereditary disorder of nervous system\Familial hemiplegic migraine\Migraine type caused by mutations in the ATP1A2 gene.
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Disorder of the central nervous system (disorder)\Disorder of brain (disorder)\Migraine with aura\Hemiplegic migraine\Familial hemiplegic migraine\Migraine type caused by mutations in the ATP1A2 gene.
\Disease\Disorder of body system\Disorder of cardiovascular system (disorder)\Cardiovascular system hereditary disorder\Familial hemiplegic migraine\Migraine type caused by mutations in the ATP1A2 gene.
\Disease\Disorder of body system\Disorder of cardiovascular system (disorder)\Vascular disorder\Vascular headache\Migraine\Migraine with aura\Hemiplegic migraine\Familial hemiplegic migraine\Migraine type caused by mutations in the ATP1A2 gene.
\Disease\Disorder of head (disorder)\Headache disorder\Vascular headache\Migraine\Migraine with aura\Hemiplegic migraine\Familial hemiplegic migraine\Migraine type caused by mutations in the ATP1A2 gene.
\Disease\Disorder of head (disorder)\Disorder of brain (disorder)\Migraine with aura\Hemiplegic migraine\Familial hemiplegic migraine\Migraine type caused by mutations in the ATP1A2 gene.
\Disease\Familial disease\Familial hemiplegic migraine\Migraine type caused by mutations in the ATP1A2 gene.
\Disease\Disorder of soft tissue\Vascular disorder\Vascular headache\Migraine\Migraine with aura\Hemiplegic migraine\Familial hemiplegic migraine\Migraine type caused by mutations in the ATP1A2 gene.

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 28-Feb 2023. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

5169711011 Migraine type caused by mutations in the ATP1A2 gene. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core

5160168013 Familial hemiplegic migraine type 2 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

5160169017 Familial hemiplegic migraine type 2 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Migraine type caused by mutations in the ATP1A2 gene.	Is a	Familial hemiplegic migraine	true	Inferred relationship	Some
Migraine type caused by mutations in the ATP1A2 gene.	Finding site	Vascular structure of head	true	Inferred relationship	Some	1
Migraine type caused by mutations in the ATP1A2 gene.	Finding site	Cerebral hemisphere structure (body structure)	true	Inferred relationship	Some	2

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
5169711011	Migraine type caused by mutations in the ATP1A2 gene.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
5160168013	Familial hemiplegic migraine type 2	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
5160169017	Familial hemiplegic migraine type 2 (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core