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1162828001: X-linked lymphoproliferative disease due to SH2D1A deficiency (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 30-Sep 2021. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
4591662013 X-linked lymphoproliferative disease due to SH2D1A deficiency (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module
4591663015 X-linked lymphoproliferative syndrome type 1 en Synonym Active Entire term case sensitive SNOMED CT core module
4591664014 SH2D1A/SLAM-associated protein deficiency en Synonym Active Entire term case sensitive SNOMED CT core module
4591665010 X-linked lymphoproliferative disease due to SH2D1A deficiency en Synonym Active Entire term case sensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
X-linked lymphoproliferative disease due to SH2D1A deficiency Is a X-linked lymphoproliferative syndrome true Inferred relationship Existential restriction modifier
X-linked lymphoproliferative disease due to SH2D1A deficiency Finding site Structure of immune system true Inferred relationship Existential restriction modifier 1
X-linked lymphoproliferative disease due to SH2D1A deficiency Associated morphology Lymphoproliferative disorder true Inferred relationship Existential restriction modifier 1
X-linked lymphoproliferative disease due to SH2D1A deficiency Pathological process Abnormal immune process true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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