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31220004: Cobalamin D disease (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
52231016 Cobalamin D disease en Synonym Active Only initial character case insensitive SNOMED CT core module
762318018 Cobalamin D disease (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module
1216348015 CblD methylmalonic acidaemia and homocystinuria en Synonym Active Entire term case sensitive SNOMED CT core module
1217848019 CblD methylmalonic acidemia and homocystinuria en Synonym Active Entire term case sensitive SNOMED CT core module
1227450016 CblD - Cobalamin locus D en Synonym Active Entire term case sensitive SNOMED CT core module
1227451017 M0E.321 Cobalamin locus D variant en Synonym Active Only initial character case insensitive SNOMED CT core module


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 Existential restriction modifier
Cobalamin D disease Occurrence Congenital false Inferred relationship Existential restriction modifier
Cobalamin D disease Finding site Body system structure false 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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