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300980002: Normocytic anemia (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
442184016 Normocytic anaemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
442185015 Normocytic anemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
696722016 Normocytic anemia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
442184016 Normocytic anaemia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
442184016 Normocytic anaemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
442185015 Normocytic anemia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
442185015 Normocytic anemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
696722016 Normocytic anemia (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
696722016 Normocytic anemia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
906771000195116 Normozytäre Anämie de Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
304071000077118 anémie normocytaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
304071000077118 anémie normocytaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
906771000195116 Normozytäre Anämie de Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

4 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Normocytic anaemia Is a Anaemia true Inferred relationship Existential restriction modifier (core metadata concept)
Normocytic anaemia Finding site Hematopoietic system structure false Inferred relationship Existential restriction modifier (core metadata concept)
Normocytic anaemia Finding site Erythrocyte false Inferred relationship Existential restriction modifier (core metadata concept)
Normocytic anaemia Finding site Hematopoietic system structure false Inferred relationship Existential restriction modifier (core metadata concept)
Normocytic anaemia Has definitional manifestation érythropénie false Inferred relationship Existential restriction modifier (core metadata concept)
Normocytic anaemia Has interpretation Below reference range false Inferred relationship Existential restriction modifier (core metadata concept) 1
Normocytic anaemia Interprets Measurement of total haemoglobin concentration false Inferred relationship Existential restriction modifier (core metadata concept) 1
Normocytic anaemia Has interpretation Below reference range false Inferred relationship Existential restriction modifier (core metadata concept) 2
Normocytic anaemia Interprets Red blood cell count false Inferred relationship Existential restriction modifier (core metadata concept) 2
Inbound Relationships Type Active Source Characteristic Refinability Group
Normocytic anemia due to aplasia Is a True Normocytic anaemia Inferred relationship Existential restriction modifier (core metadata concept)
Normocytic anaemia following acute bleed Is a True Normocytic anaemia Inferred relationship Existential restriction modifier (core metadata concept)
Normocytic anaemia due to chronic blood loss Is a True Normocytic anaemia Inferred relationship Existential restriction modifier (core metadata concept)
A rare congenital disorder of glycosylation caused by mutations in the CAD gene and characterized by epileptic encephalopathy, global developmental delay, normocytic anemia and anisopoikilocytosis. Loss of acquired skills in early childhood is present and natural disease course can be lethal in early childhood. Is a True Normocytic anaemia Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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