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1153403009: Hereditary iron deficiency anemia (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
4564223017 Hereditary iron deficiency anemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4564224011 Hereditary iron deficiency anemia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4564225012 Hereditary iron deficiency anaemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4564223017 Hereditary iron deficiency anemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4564224011 Hereditary iron deficiency anemia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4564225012 Hereditary iron deficiency anaemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
6257681000241115 anémie héréditaire par carence martiale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6257691000241118 anémie ferriprive héréditaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6257701000241118 anémie héréditaire par carence en fer fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6257681000241115 anémie héréditaire par carence martiale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6257691000241118 anémie ferriprive héréditaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6257701000241118 anémie héréditaire par carence en fer fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hereditary iron deficiency anemia Due to Iron deficiency (disorder) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Hereditary iron deficiency anemia Has interpretation Below reference range true Inferred relationship Existential restriction modifier (core metadata concept) 1
Hereditary iron deficiency anemia Is a Hereditary disease true Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary iron deficiency anemia Interprets Measurement of total haemoglobin concentration true Inferred relationship Existential restriction modifier (core metadata concept) 1
Hereditary iron deficiency anemia Has interpretation Below reference range true Inferred relationship Existential restriction modifier (core metadata concept) 3
Hereditary iron deficiency anemia Interprets Red blood cell count true Inferred relationship Existential restriction modifier (core metadata concept) 3
Hereditary iron deficiency anemia Is a Iron deficiency anemia true Inferred relationship Existential restriction modifier (core metadata concept)

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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