FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.13  |  FHIR Version n/a  User: [n/a]

69614003: Adenosylcobalamin synthesis defect (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
115650017 Adenosylcobalamin synthesis defect en Synonym Active Case insensitive SNOMED CT core
115652013 Methylmalonic aciduria, type II en Synonym Active Initial character case insensitive SNOMED CT core
1216875018 Methylmalonic acidaemia due to defects in adenosylcobalamin biosynthesis en Synonym Active Case insensitive SNOMED CT core
1216877014 Vitamin B12-responsive methylmalonic acidaemia en Synonym Active Initial character case insensitive SNOMED CT core
1218362019 Methylmalonic acidemia due to defects in adenosylcobalamin biosynthesis en Synonym Active Case insensitive SNOMED CT core
1218363012 Vitamin B12-responsive methylmalonic acidemia en Synonym Active Initial character case insensitive SNOMED CT core
809579010 Adenosylcobalamin synthesis defect (disorder) en Fully specified name Active Case insensitive SNOMED CT core


2 descendants. Search Descendants:

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group
Cobalamin A disease Is a True Adenosylcobalamin synthesis defect Inferred relationship Some
Cobalamin B disease Is a True Adenosylcobalamin synthesis defect Inferred relationship Some

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

Back to Start