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238003000: Carnitine acylcarnitine translocase deficiency (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
356730018 Carnitine acylcarnitine translocase deficiency en Synonym Active Entire term case insensitive SNOMED CT core module
626819017 Carnitine acylcarnitine translocase deficiency (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
Carnitine acylcarnitine translocase deficiency Is a Disorder of fatty acid metabolism false Inferred relationship Existential restriction modifier
Carnitine acylcarnitine translocase deficiency Finding site Body system structure false Inferred relationship Existential restriction modifier
Carnitine acylcarnitine translocase deficiency Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Carnitine acylcarnitine translocase deficiency Is a Fatty acid oxidation defect true Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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