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31220004: Cobalamin D disease (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
1216348015 CblD methylmalonic acidaemia and homocystinuria en Synonym Active Case sensitive SNOMED CT core
1217848019 CblD methylmalonic acidemia and homocystinuria en Synonym Active Case sensitive SNOMED CT core
1227450016 CblD - Cobalamin locus D en Synonym Active Case sensitive SNOMED CT core
1227451017 M0E.321 Cobalamin locus D variant en Synonym Active Initial character case insensitive SNOMED CT core
52231016 Cobalamin D disease en Synonym Active Initial character case insensitive SNOMED CT core
762318018 Cobalamin D disease (disorder) en Fully specified name Active Initial character case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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