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95656000: Familial hemiplegic migraine (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
158462010 Familial hemiplegic migraine en Synonym Active Entire term case insensitive SNOMED CT core module
158463017 Hemiplegic-ophthalmoplegic migraine en Synonym Active Entire term case insensitive SNOMED CT core module
839855018 Familial hemiplegic migraine (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Familial hemiplegic migraine Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Familial hemiplegic migraine Is a Familial disease true Inferred relationship Existential restriction modifier
Familial hemiplegic migraine Is a Hereditary disorder of nervous system true Inferred relationship Existential restriction modifier
Familial hemiplegic migraine Is a Hemiplegic migraine true Inferred relationship Existential restriction modifier
Familial hemiplegic migraine Finding site Structure of telencephalon false Inferred relationship Existential restriction modifier
Familial hemiplegic migraine Finding site Cerebral hemisphere structure true Inferred relationship Existential restriction modifier 1
Familial hemiplegic migraine Is a Cardiovascular system hereditary disorder true Inferred relationship Existential restriction modifier
Familial hemiplegic migraine Has definitional manifestation Headache false Inferred relationship Existential restriction modifier
Familial hemiplegic migraine Finding site Vascular structure of head true Inferred relationship Existential restriction modifier 2
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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