702450004: FOXG1 syndrome (disorder)

SNOMED CT Concept\constatation clinique\...

\constatation à propos du système nerveux central\constatation à propos l'encéphale\Disorder of brain (disorder)\anomalie congénitale de l'encéphale\FOXG1 syndrome
\constatation à propos du système nerveux central\Disorder of the central nervous system (disorder)\Congenital anomaly of central nervous system\anomalie congénitale de l'encéphale\FOXG1 syndrome
\constatation à propos du système nerveux central\Disorder of the central nervous system (disorder)\Disorder of brain (disorder)\anomalie congénitale de l'encéphale\FOXG1 syndrome

\constatation à propos d'une région de la tête et du cou\Head finding (finding)\...

\constatation à propos l'encéphale\Disorder of brain (disorder)\anomalie congénitale de l'encéphale\FOXG1 syndrome

\affection de la tête\Congenital anomaly of head\anomalie congénitale de l'encéphale\FOXG1 syndrome
\affection de la tête\Disorder of brain (disorder)\anomalie congénitale de l'encéphale\FOXG1 syndrome

\Disease\Genetic disease\maladie héréditaire\Hereditary disorder by system\Hereditary disorder of nervous system\FOXG1 syndrome
\Disease\Genetic disease\maladie héréditaire\Developmental hereditary disorder\FOXG1 syndrome
\Disease\Genetic disease\maladie héréditaire\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\FOXG1 syndrome
\Disease\affection d'un système corporel\Hereditary disorder by system\Hereditary disorder of nervous system\FOXG1 syndrome
\Disease\affection d'un système corporel\Disorder of nervous system (disorder)\Hereditary disorder of nervous system\FOXG1 syndrome
\Disease\affection d'un système corporel\Disorder of nervous system (disorder)\Congenital anomaly of nervous system\Congenital anomaly of central nervous system\anomalie congénitale de l'encéphale\FOXG1 syndrome
\Disease\affection d'un système corporel\Disorder of nervous system (disorder)\Disorder of the central nervous system (disorder)\Congenital anomaly of central nervous system\anomalie congénitale de l'encéphale\FOXG1 syndrome
\Disease\affection d'un système corporel\Disorder of nervous system (disorder)\Disorder of the central nervous system (disorder)\Disorder of brain (disorder)\anomalie congénitale de l'encéphale\FOXG1 syndrome
\Disease\affection de la tête\Congenital anomaly of head\anomalie congénitale de l'encéphale\FOXG1 syndrome
\Disease\affection de la tête\Disorder of brain (disorder)\anomalie congénitale de l'encéphale\FOXG1 syndrome
\Disease\trouble mental\troubles mentaux du développement\Disorder of psychological development\Autism spectrum disorder\FOXG1 syndrome
\Disease\Congenital disease\Congenital malformation\Congenital anomaly of nervous system\Congenital anomaly of central nervous system\anomalie congénitale de l'encéphale\FOXG1 syndrome
\Disease\Congenital disease\Congenital malformation\Congenital anomaly of head\anomalie congénitale de l'encéphale\FOXG1 syndrome
\Disease\trouble du développement\Neurodevelopmental disorder\troubles mentaux du développement\Disorder of psychological development\Autism spectrum disorder\FOXG1 syndrome
\Disease\trouble du développement\Developmental hereditary disorder\FOXG1 syndrome
\Disease\trouble du développement\Congenital malformation\Congenital anomaly of nervous system\Congenital anomaly of central nervous system\anomalie congénitale de l'encéphale\FOXG1 syndrome
\Disease\trouble du développement\Congenital malformation\Congenital anomaly of head\anomalie congénitale de l'encéphale\FOXG1 syndrome

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2014. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

2995373012 FOXG1 syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

3038730013 FOXG1 syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
FOXG1 syndrome	Pathological process (attribute)	Pathological developmental process	false	Inferred relationship	Some	3
FOXG1 syndrome	Pathological process (attribute)	Pathological developmental process	true	Inferred relationship	Some	1
FOXG1 syndrome	est un(e) (attribut)	anomalie congénitale de l'encéphale	true	Inferred relationship	Some
FOXG1 syndrome	morphologie associée (attribut)	structure anormale sur le plan morphologique	true	Inferred relationship	Some	1
FOXG1 syndrome	localisation d'une constatation (attribut)	structure de l'encéphale	true	Inferred relationship	Some	1
FOXG1 syndrome	est un(e) (attribut)	Developmental hereditary disorder	true	Inferred relationship	Some
FOXG1 syndrome	est un(e) (attribut)	Autosomal dominant hereditary disorder	true	Inferred relationship	Some
FOXG1 syndrome	est un(e) (attribut)	Congenital disease	false	Inferred relationship	Some
FOXG1 syndrome	est un(e) (attribut)	Disorder of brain (disorder)	false	Inferred relationship	Some
FOXG1 syndrome	est un(e) (attribut)	Hereditary disorder of nervous system	true	Inferred relationship	Some
FOXG1 syndrome	est un(e) (attribut)	Autism spectrum disorder	true	Inferred relationship	Some
FOXG1 syndrome	survenue (attribut)	congénital	true	Inferred relationship	Some	1
FOXG1 syndrome	localisation d'une constatation (attribut)	structure de l'encéphale	false	Inferred relationship	Some	2

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
PPM-X syndrome	est un(e) (attribut)	False	FOXG1 syndrome	Inferred relationship	Some

Reference Sets

Canada English language reference set (foundation metadata concept)

GB English

US English

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
2995373012	FOXG1 syndrome	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
3038730013	FOXG1 syndrome (disorder)	en	Fully specified name	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core