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723508002: RAS-associated autoimmune leukoproliferative disease (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3424876017 RAS-associated autoimmune leukoproliferative disease (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
3424877014 RAS-associated autoimmune leukoproliferative disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3424878016 RAS-associated autoimmune leucoproliferative disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3424879012 Autoimmune lymphoproliferative syndrome type 4 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3424880010 Autoimmune lymphoproliferative syndrome type IV en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3424881014 RALD - RAS-associated autoimmune leukoproliferative disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3424882019 RALD - RAS-associated autoimmune leucoproliferative disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5403095014 RAS-associated autoimmune leukoproliferative disease (RALD) is a rare genetic disorder characterized by monocytosis, autoimmune cytopenias, lymphoproliferation, hepatosplenomegaly, and hypergammaglobulinemia. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5403096010 RAS-associated autoimmune leucoproliferative disease (RALD) is a rare genetic disorder characterised by monocytosis, autoimmune cytopenias, lymphoproliferation, hepatosplenomegaly, and hypergammaglobulinaemia. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
RAS-associated autoimmune leukoproliferative disease (disorder) Due to Chromosomal disorder (disorder) true Inferred relationship Some 2
RAS-associated autoimmune leukoproliferative disease (disorder) Is a Autoimmune disease true Inferred relationship Some
RAS-associated autoimmune leukoproliferative disease (disorder) Is a Immunodeficiency associated with chromosomal abnormality true Inferred relationship Some
RAS-associated autoimmune leukoproliferative disease (disorder) Is a Lymphoproliferative disorder true Inferred relationship Some
RAS-associated autoimmune leukoproliferative disease (disorder) Is a Hereditary cancer-predisposing syndrome true Inferred relationship Some
RAS-associated autoimmune leukoproliferative disease (disorder) Has definitional manifestation Immune system finding false Inferred relationship Some
RAS-associated autoimmune leukoproliferative disease (disorder) Associated morphology Lymphoproliferative disorder (morphologic abnormality) true Inferred relationship Some 4
RAS-associated autoimmune leukoproliferative disease (disorder) Pathological process (attribute) Autoimmune process true Inferred relationship Some 4

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

GB English

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