702450004: FOXG1 syndrome (disorder)

SNOMED CT Concept\Clinical finding\...

\Central nervous system finding\Finding of brain\Disorder of brain\Congenital anomaly of brain\FOXG1 syndrome
\Central nervous system finding\Disorder of the central nervous system\Congenital anomaly of central nervous system\Congenital anomaly of brain\FOXG1 syndrome
\Central nervous system finding\Disorder of the central nervous system\Disorder of brain\Congenital anomaly of brain\FOXG1 syndrome

\Finding of head and neck region\Head finding\...

\Finding of brain\Disorder of brain\Congenital anomaly of brain\FOXG1 syndrome

\Disorder of head\Congenital anomaly of head\Congenital anomaly of brain\FOXG1 syndrome
\Disorder of head\Disorder of brain\Congenital anomaly of brain\FOXG1 syndrome

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of nervous system\FOXG1 syndrome
\Disease\Genetic disease\Hereditary disease\Developmental hereditary disorder\FOXG1 syndrome
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\FOXG1 syndrome
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of nervous system\FOXG1 syndrome
\Disease\Disorder of body system\Disorder of nervous system\Hereditary disorder of nervous system\FOXG1 syndrome
\Disease\Disorder of body system\Disorder of nervous system\Congenital anomaly of nervous system\Congenital anomaly of central nervous system\Congenital anomaly of brain\FOXG1 syndrome
\Disease\Disorder of body system\Disorder of nervous system\Disorder of the central nervous system\Congenital anomaly of central nervous system\Congenital anomaly of brain\FOXG1 syndrome
\Disease\Disorder of body system\Disorder of nervous system\Disorder of the central nervous system\Disorder of brain\Congenital anomaly of brain\FOXG1 syndrome
\Disease\Disorder of head\Congenital anomaly of head\Congenital anomaly of brain\FOXG1 syndrome
\Disease\Disorder of head\Disorder of brain\Congenital anomaly of brain\FOXG1 syndrome
\Disease\Mental disorder\Developmental mental disorder\Disorder of psychological development\Pervasive developmental disorder\FOXG1 syndrome
\Disease\Congenital disease\Congenital malformation\Congenital anomaly of nervous system\Congenital anomaly of central nervous system\Congenital anomaly of brain\FOXG1 syndrome
\Disease\Congenital disease\Congenital malformation\Congenital anomaly of head\Congenital anomaly of brain\FOXG1 syndrome
\Disease\Developmental disorder\Neurodevelopmental disorder\Developmental mental disorder\Disorder of psychological development\Pervasive developmental disorder\FOXG1 syndrome
\Disease\Developmental disorder\Developmental hereditary disorder\FOXG1 syndrome
\Disease\Developmental disorder\Congenital malformation\Congenital anomaly of nervous system\Congenital anomaly of central nervous system\Congenital anomaly of brain\FOXG1 syndrome
\Disease\Developmental disorder\Congenital malformation\Congenital anomaly of head\Congenital anomaly of brain\FOXG1 syndrome

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

Descriptions:

Id Description Lang Type Status Case? Module

2995373012 FOXG1 syndrome en Synonym Active Entire term case sensitive SNOMED CT core module

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

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
FOXG1 syndrome	Is a	Autosomal dominant hereditary disorder	true	Inferred relationship	Existential restriction modifier
FOXG1 syndrome	Is a	Congenital disease	false	Inferred relationship	Existential restriction modifier
FOXG1 syndrome	Is a	Disorder of brain	false	Inferred relationship	Existential restriction modifier
FOXG1 syndrome	Is a	Hereditary disorder of nervous system	true	Inferred relationship	Existential restriction modifier
FOXG1 syndrome	Is a	Pervasive developmental disorder	true	Inferred relationship	Existential restriction modifier
FOXG1 syndrome	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	1
FOXG1 syndrome	Finding site	Brain structure	false	Inferred relationship	Existential restriction modifier	2
FOXG1 syndrome	Pathological process	Pathological developmental process	false	Inferred relationship	Existential restriction modifier	3
FOXG1 syndrome	Pathological process	Pathological developmental process	true	Inferred relationship	Existential restriction modifier	1
FOXG1 syndrome	Is a	Congenital anomaly of brain	true	Inferred relationship	Existential restriction modifier
FOXG1 syndrome	Associated morphology	Morphologically abnormal structure	true	Inferred relationship	Existential restriction modifier	1
FOXG1 syndrome	Finding site	Brain structure	true	Inferred relationship	Existential restriction modifier	1
FOXG1 syndrome	Is a	Developmental hereditary disorder	true	Inferred relationship	Existential restriction modifier

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
X-linked intellectual disability-psychosis-macroorchidism syndrome	Is a	False	FOXG1 syndrome	Inferred relationship	Existential restriction modifier

This concept is not in any reference sets

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