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1260327007: Familial hemiplegic migraine type 3 (disorder)


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
5169712016 Migraine type caused by mutations in the SCN1A gene. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5160162014 Familial hemiplegic migraine type 3 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5160163016 Familial hemiplegic migraine type 3 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Migraine type caused by mutations in the SCN1A gene. Is a Familial hemiplegic migraine true Inferred relationship Some
Migraine type caused by mutations in the SCN1A gene. Finding site Vascular structure of head true Inferred relationship Some 1
Migraine type caused by mutations in the SCN1A 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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