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53881000052103: Hereditary hypogammaglobulinemia (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Nov 2015. Module: SNOMED CT Sweden NRC maintained module (core metadata concept)

Descriptions:

Id Description Lang Type Status Case? Module Reference Sets
3813031000052113 Hereditary hypogammaglobulinemia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept) GB English: Preferred (foundation metadata concept)
3813041000052119 Hereditary hypogammaglobulinemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept) US English: Preferred (foundation metadata concept)
3813051000052116 Hereditary hypogammaglobulinaemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept) GB English: Preferred (foundation metadata concept)
3813061000052118 hereditär hypogammaglobulinemi sv Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept) Swedish [International Organization for Standardization 639-1 code sv] language reference set (foundation metadata concept): Preferred (foundation metadata concept)

0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hereditary hypogammaglobulinemia (disorder) Is a Hereditary disease true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Medical conditions, alert information reference set (foundation metadata concept)

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