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1260330000: Familial hemiplegic migraine type 2 (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
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
5169711011 Migraine type caused by mutations in the ATP1A2 gene. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Familial hemiplegic migraine type 2 Is a Familial hemiplegic migraine true Inferred relationship Some
Familial hemiplegic migraine type 2 Finding site Vascular structure of head true Inferred relationship Some 1
Familial hemiplegic migraine type 2 Finding site Cerebral hemisphere structure (body structure) true Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

GB English

US English

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