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448227009: X-linked periventricular heterotopia (disorder)

SNOMED CT Concept\Clinical finding\...

\Neurological lesion\Neuronal heterotopia\X-linked periventricular heterotopia

\Central nervous system finding\Disorder of the central nervous system\Congenital anomaly of central nervous system\Disorder of neuronal migration and differentiation\Neuronal heterotopia\X-linked periventricular heterotopia

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of nervous system\X-linked periventricular heterotopia
\Disease\Genetic disease\Hereditary disease\Developmental hereditary disorder\X-linked periventricular heterotopia
\Disease\Genetic disease\Hereditary disease\Sex-linked hereditary disorder\X-linked hereditary disease\X-linked periventricular heterotopia
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of nervous system\X-linked periventricular heterotopia
\Disease\Disorder of body system\Disorder of nervous system\Hereditary disorder of nervous system\X-linked periventricular heterotopia
\Disease\Disorder of body system\Disorder of nervous system\Congenital anomaly of nervous system\Congenital anomaly of central nervous system\Disorder of neuronal migration and differentiation\Neuronal heterotopia\X-linked periventricular heterotopia
\Disease\Disorder of body system\Disorder of nervous system\Disorder of the central nervous system\Congenital anomaly of central nervous system\Disorder of neuronal migration and differentiation\Neuronal heterotopia\X-linked periventricular heterotopia
\Disease\Congenital disease\Congenital malformation\Congenital anomaly of nervous system\Congenital anomaly of central nervous system\Disorder of neuronal migration and differentiation\Neuronal heterotopia\X-linked periventricular heterotopia
\Disease\Developmental disorder\Developmental hereditary disorder\X-linked periventricular heterotopia
\Disease\Developmental disorder\Congenital malformation\Congenital anomaly of nervous system\Congenital anomaly of central nervous system\Disorder of neuronal migration and differentiation\Neuronal heterotopia\X-linked periventricular heterotopia

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2011. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module

2899028015 X-linked periventricular heterotopia (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module

2901567019 PVH - Periventricular heterotopia en Synonym Active Only initial character case insensitive SNOMED CT core module

2901568012 X-linked periventricular heterotopia en Synonym Active Entire term case sensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
X-linked periventricular heterotopia	Is a	X-linked hereditary disease	true	Inferred relationship	Existential restriction modifier
X-linked periventricular heterotopia	Is a	Hereditary disorder of nervous system	true	Inferred relationship	Existential restriction modifier
X-linked periventricular heterotopia	Is a	Neuronal heterotopia	true	Inferred relationship	Existential restriction modifier
X-linked periventricular heterotopia	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier
X-linked periventricular heterotopia	Finding site	Structure of central nervous system	false	Inferred relationship	Existential restriction modifier	1
X-linked periventricular heterotopia	Associated morphology	Neuronal heterotopia	true	Inferred relationship	Existential restriction modifier	1
X-linked periventricular heterotopia	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier	2
X-linked periventricular heterotopia	Finding site	Structure of central nervous system	false	Inferred relationship	Existential restriction modifier	3
X-linked periventricular heterotopia	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier	3
X-linked periventricular heterotopia	Finding site	Structure of central nervous system	false	Inferred relationship	Existential restriction modifier	4
X-linked periventricular heterotopia	Associated morphology	Developmental anomaly	false	Inferred relationship	Existential restriction modifier	2
X-linked periventricular heterotopia	Finding site	Structure of nervous system	false	Inferred relationship	Existential restriction modifier	2
X-linked periventricular heterotopia	Associated morphology	Congenital anomaly	false	Inferred relationship	Existential restriction modifier	4
X-linked periventricular heterotopia	Associated morphology	Neuronal heterotopia	false	Inferred relationship	Existential restriction modifier	3
X-linked periventricular heterotopia	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	1
X-linked periventricular heterotopia	Associated morphology	Developmental anomaly	false	Inferred relationship	Existential restriction modifier	1
X-linked periventricular heterotopia	Finding site	Structure of central nervous system	true	Inferred relationship	Existential restriction modifier	1
X-linked periventricular heterotopia	Pathological process	Pathological developmental process	true	Inferred relationship	Existential restriction modifier	1
X-linked periventricular heterotopia	Is a	Developmental hereditary disorder	true	Inferred relationship	Existential restriction modifier

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
2899028015	X-linked periventricular heterotopia (disorder)	en	Fully specified name	Active	Entire term case sensitive	SNOMED CT core module
2901567019	PVH - Periventricular heterotopia	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
2901568012	X-linked periventricular heterotopia	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module