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50715003: Pure red cell aplasia (disorder)

Status: current, Defined. Date: 31-Jul 2016. Module: SNOMED CT core

Descriptions:

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

7 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Pure red cell aplasia Is a RBC count low true Inferred relationship Some
Pure red cell aplasia Is a Anaemia true Inferred relationship Some
Pure red cell aplasia Finding site Bone marrow structure false Inferred relationship Some 1
Pure red cell aplasia Has definitional manifestation Decreased erythrocyte production false Inferred relationship Some
Pure red cell aplasia Has definitional manifestation Erythropenia false Inferred relationship Some
Pure red cell aplasia Is a Anaemia due to decreased red cell production false Inferred relationship Some
Pure red cell aplasia Is a Aplastic anaemia false Inferred relationship Some
Pure red cell aplasia Is a Anaemia due to disturbance of proliferation AND/OR differentiation of erythroid precursor cells false Inferred relationship Some
Pure red cell aplasia Finding site Bone structure false Inferred relationship Some
Pure red cell aplasia Associated morphology Aplasia false Inferred relationship Some 1
Pure red cell aplasia Finding site Bone marrow structure false Inferred relationship Some 1
Pure red cell aplasia Due to Decreased erythrocyte production false Inferred relationship Some
Pure red cell aplasia Associated morphology Aplasia true Inferred relationship Some 2
Pure red cell aplasia Finding site Structure of erythropoietic tissue true Inferred relationship Some 2
Pure red cell aplasia Interprets Decreased erythrocyte production false Inferred relationship Some
Pure red cell aplasia Finding site Haematopoietic system structure false Inferred relationship Some
Pure red cell aplasia Finding site Erythrocyte false Inferred relationship Some
Pure red cell aplasia Associated morphology Aplasia false Inferred relationship Some 1
Pure red cell aplasia Finding site Entire haematological system false Inferred relationship Some 1
Pure red cell aplasia Interprets Red blood cell count true Inferred relationship Some 1
Pure red cell aplasia Is a Blood disease false Inferred relationship Some
Pure red cell aplasia Interprets Haematology procedure false Inferred relationship Some 3
Pure red cell aplasia Has interpretation Below reference range true Inferred relationship Some 1
Pure red cell aplasia Is a Bone marrow disorder true Inferred relationship Some
Pure red cell aplasia Is a Erythropenia false Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Acute pure red cell aplasia Is a True Pure red cell aplasia Inferred relationship Some
Congenital hypoplastic anaemia Is a False Pure red cell aplasia Inferred relationship Some
Pure red cell aplasia, acquired Is a False Pure red cell aplasia Inferred relationship Some
Congenital pure red cell aplasia Is a False Pure red cell aplasia Inferred relationship Some
Constitutional red cell aplasia and hypoplasia Is a False Pure red cell aplasia Inferred relationship Some
Secondary red cell aplasia NEC Is a False Pure red cell aplasia Inferred relationship Some
Transient erythroblastopenia of childhood Is a True Pure red cell aplasia Inferred relationship Some
Acquired red cell aplasia Is a True Pure red cell aplasia Inferred relationship Some

Reference Sets

Clinical manifestation reference set

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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