773668008: Childhood encephalopathy due to thiamine pyrophosphokinase deficiency (disorder)

Descriptions:

Id Description Lang Type Status Case? Module

3725649018 Childhood encephalopathy due to thiamine pyrophosphokinase deficiency (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

3725650018 Childhood encephalopathy due to thiamine pyrophosphokinase deficiency en Synonym Active Entire term case insensitive SNOMED CT core module

3725651019 Childhood encephalopathy due to thiamin pyrophosphokinase deficiency en Synonym Active Entire term case insensitive SNOMED CT core module

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Childhood encephalopathy due to thiamine pyrophosphokinase deficiency	Occurrence	Childhood	true	Inferred relationship	Existential restriction modifier	1
Childhood encephalopathy due to thiamine pyrophosphokinase deficiency	Is a	Metabolic encephalopathy	true	Inferred relationship	Existential restriction modifier
Childhood encephalopathy due to thiamine pyrophosphokinase deficiency	Due to	Deficiency of thiamine pyrophosphokinase	true	Inferred relationship	Existential restriction modifier	2
Childhood encephalopathy due to thiamine pyrophosphokinase deficiency	Is a	Autosomal recessive hereditary disorder	true	Inferred relationship	Existential restriction modifier
Childhood encephalopathy due to thiamine pyrophosphokinase deficiency	Is a	Hereditary disorder of nervous system	true	Inferred relationship	Existential restriction modifier
Childhood encephalopathy due to thiamine pyrophosphokinase deficiency	Finding site	Brain structure	true	Inferred relationship	Existential restriction modifier	1
Childhood encephalopathy due to thiamine pyrophosphokinase deficiency	Is a	Central nervous system complication	true	Inferred relationship	Existential restriction modifier

Inbound Relationships

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Active

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Characteristic

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This concept is not in any reference sets

Id	Description	Lang	Type	Status	Case?	Module
3725649018	Childhood encephalopathy due to thiamine pyrophosphokinase deficiency (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module
3725650018	Childhood encephalopathy due to thiamine pyrophosphokinase deficiency	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
3725651019	Childhood encephalopathy due to thiamin pyrophosphokinase deficiency	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module