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4409006: Adenosylcobalamin and methylcobalamin synthesis defect (disorder)


Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
493787010 Combined methylmalonic acidaemia and homocystinuria due to defects in adenosylcobalamin and methylcobalamin synthesis en Synonym Active Case insensitive SNOMED CT core
493788017 Combined methylmalonic acidemia and homocystinuria due to defects in adenosylcobalamin and methylcobalamin synthesis en Synonym Active Case insensitive SNOMED CT core
7715018 Adenosylcobalamin and methylcobalamin synthesis defect en Synonym Active Case insensitive SNOMED CT core
781178011 Adenosylcobalamin and methylcobalamin synthesis defect (disorder) en Fully specified name Active Case insensitive SNOMED CT core


4 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Adenosylcobalamin and methylcobalamin synthesis defect Is a Methylmalonic acidaemia true Inferred relationship Some
Adenosylcobalamin and methylcobalamin synthesis defect Occurrence Congenital false Inferred relationship Some
Adenosylcobalamin and methylcobalamin synthesis defect Finding site Body system structure false Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Cobalamin D disease Is a True Adenosylcobalamin and methylcobalamin synthesis defect Inferred relationship Some
Cobalamin A disease Is a True Adenosylcobalamin and methylcobalamin synthesis defect Inferred relationship Some
Cobalamin C disease Is a True Adenosylcobalamin and methylcobalamin synthesis defect Inferred relationship Some
Inherited methylmalonic acidaemia AND homocystinuria Is a True Adenosylcobalamin and methylcobalamin synthesis defect Inferred relationship Some

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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