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50715003: Pure red cell aplasia (disorder)


Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jul 2016. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
84523015 Pure red cell aplasia en Synonym Active Entire term case insensitive SNOMED CT core module
84526011 Primary red cell aplasia en Synonym Active Entire term case insensitive SNOMED CT core module
84527019 Pure red cell anemia en Synonym Active Entire term case insensitive SNOMED CT core module
495763010 Red cell hypoplasia en Synonym Active Entire term case insensitive SNOMED CT core module
495764016 Pure red cell anaemia en Synonym Active Entire term case insensitive SNOMED CT core module
788534016 Pure red cell aplasia (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module


7 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Pure red cell aplasia Is a Anemia due to decreased red cell production false Inferred relationship Existential restriction modifier
Pure red cell aplasia Is a Aplastic anemia false Inferred relationship Existential restriction modifier
Pure red cell aplasia Is a Anemia due to disturbance of proliferation AND/OR differentiation of erythroid precursor cells false Inferred relationship Existential restriction modifier
Pure red cell aplasia Interprets Decreased erythrocyte production false Inferred relationship Existential restriction modifier
Pure red cell aplasia Finding site Hematopoietic system structure false Inferred relationship Existential restriction modifier
Pure red cell aplasia Finding site Erythrocyte false Inferred relationship Existential restriction modifier
Pure red cell aplasia Associated morphology Aplasia false Inferred relationship Existential restriction modifier 1
Pure red cell aplasia Finding site Entire hematological system false Inferred relationship Existential restriction modifier 1
Pure red cell aplasia Finding site Bone marrow structure false Inferred relationship Existential restriction modifier 1
Pure red cell aplasia Has definitional manifestation Decreased erythrocyte production false Inferred relationship Existential restriction modifier
Pure red cell aplasia Has definitional manifestation Erythropenia false Inferred relationship Existential restriction modifier
Pure red cell aplasia Finding site Bone structure false Inferred relationship Existential restriction modifier
Pure red cell aplasia Associated morphology Aplasia false Inferred relationship Existential restriction modifier 1
Pure red cell aplasia Finding site Bone marrow structure false Inferred relationship Existential restriction modifier 1
Pure red cell aplasia Due to Decreased erythrocyte production false Inferred relationship Existential restriction modifier
Pure red cell aplasia Associated morphology Aplasia true Inferred relationship Existential restriction modifier 2
Pure red cell aplasia Finding site Structure of erythropoietic tissue true Inferred relationship Existential restriction modifier 2
Pure red cell aplasia Interprets Red blood cell count true Inferred relationship Existential restriction modifier 1
Pure red cell aplasia Is a Disorder of cellular component of blood false Inferred relationship Existential restriction modifier
Pure red cell aplasia Interprets Hematology procedure false Inferred relationship Existential restriction modifier 3
Pure red cell aplasia Has interpretation Below reference range true Inferred relationship Existential restriction modifier 1
Pure red cell aplasia Is a Bone marrow disorder true Inferred relationship Existential restriction modifier
Pure red cell aplasia Is a Erythropenia false Inferred relationship Existential restriction modifier
Pure red cell aplasia Is a Red blood cell count below reference range true Inferred relationship Existential restriction modifier
Pure red cell aplasia Is a Anemia true Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group
Transient erythroblastopenia of childhood Is a True Pure red cell aplasia Inferred relationship Existential restriction modifier
Acquired red cell aplasia Is a True Pure red cell aplasia Inferred relationship Existential restriction modifier
Acute pure red cell aplasia Is a True Pure red cell aplasia Inferred relationship Existential restriction modifier
Congenital hypoplastic anemia Is a False Pure red cell aplasia Inferred relationship Existential restriction modifier
Pure red cell aplasia, acquired Is a False Pure red cell aplasia Inferred relationship Existential restriction modifier
Congenital pure red cell aplasia Is a False Pure red cell aplasia Inferred relationship Existential restriction modifier
Constitutional red cell aplasia and hypoplasia Is a False Pure red cell aplasia Inferred relationship Existential restriction modifier
Secondary red cell aplasia NEC Is a False Pure red cell aplasia Inferred relationship Existential restriction modifier
Secondary red cell aplasia NEC Is a False Pure red cell aplasia Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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