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1351781002: Autosomal recessive combined immunodeficiency due to BCL10 immune signaling adaptor mutation (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 01-Dec 2024. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
5415033013 Autosomal recessive combined immunodeficiency due to BCL10 mutation en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5415034019 Autosomal recessive combined immunodeficiency due to BCL10 immune signaling adaptor mutation en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5415035018 Autosomal recessive combined immunodeficiency due to BCL10 immune signaling adaptor mutation (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5415036017 Autosomal recessive combined immunodeficiency due to BCL10 deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Autosomal recessive combined immunodeficiency due to BCL10 mutation Is a Combined immunodeficiency disease true Inferred relationship Some
Autosomal recessive combined immunodeficiency due to BCL10 mutation Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Autosomal recessive combined immunodeficiency due to BCL10 mutation Pathological process (attribute) Abnormal immune process (qualifier value) true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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