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74653006: Cobalamin C disease (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
1216917016 CblC methylmalonic acidaemia and homocystinuria en Synonym Active Case sensitive SNOMED CT core
1218404017 CblC methylmalonic acidemia and homocystinuria en Synonym Active Case sensitive SNOMED CT core
1233773015 Cobalamin locus C variant en Synonym Active Initial character case insensitive SNOMED CT core
1233774014 CblC - Cobalamin locus C en Synonym Active Case sensitive SNOMED CT core
123975018 Cobalamin C disease en Synonym Active Initial character case insensitive SNOMED CT core
815176014 Cobalamin C 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 C disease Is a Adenosylcobalamin and methylcobalamin synthesis defect true Inferred relationship Some
Cobalamin C disease Finding site Body system structure false Inferred relationship Some
Cobalamin C disease Occurrence Congenital 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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