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60504009: Megaloblastic anemia due to congenital deficiency of intrinsic factor (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2003. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
100530016 Megaloblastic anemia due to congenital deficiency of intrinsic factor en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
100531017 Congenital intrinsic factor deficiency anemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
498762018 Megaloblastic anaemia due to congenital deficiency of intrinsic factor en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
498763011 Congenital intrinsic factor deficiency anaemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
799464015 Megaloblastic anemia due to congenital deficiency of intrinsic factor (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
100530016 Megaloblastic anemia due to congenital deficiency of intrinsic factor en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
100530016 Megaloblastic anemia due to congenital deficiency of intrinsic factor en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
100531017 Congenital intrinsic factor deficiency anemia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
100531017 Congenital intrinsic factor deficiency anemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
498762018 Megaloblastic anaemia due to congenital deficiency of intrinsic factor en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
498762018 Megaloblastic anaemia due to congenital deficiency of intrinsic factor en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
498763011 Congenital intrinsic factor deficiency anaemia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
498763011 Congenital intrinsic factor deficiency anaemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
799464015 Megaloblastic anemia due to congenital deficiency of intrinsic factor (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
799464015 Megaloblastic anemia due to congenital deficiency of intrinsic factor (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4588411000241116 anémie mégaloblastique par déficit congénital en facteur intrinsèque fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
4588411000241116 anémie mégaloblastique par déficit congénital en facteur intrinsèque 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
Megaloblastic anaemia due to congenital deficiency of intrinsic factor Is a Megaloblastic anaemia due to inborn errors of metabolism true Inferred relationship Existential restriction modifier (core metadata concept)
Megaloblastic anaemia due to congenital deficiency of intrinsic factor Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 3
Megaloblastic anaemia due to congenital deficiency of intrinsic factor Finding site Hematopoietic system structure false Inferred relationship Existential restriction modifier (core metadata concept)
Megaloblastic anaemia due to congenital deficiency of intrinsic factor Finding site Erythrocyte false Inferred relationship Existential restriction modifier (core metadata concept)
Megaloblastic anaemia due to congenital deficiency of intrinsic factor Associated etiologic finding Congenital deficiency of intrinsic factor false Inferred relationship Existential restriction modifier (core metadata concept)
Megaloblastic anaemia due to congenital deficiency of intrinsic factor Has definitional manifestation érythropénie false Inferred relationship Existential restriction modifier (core metadata concept)
Megaloblastic anaemia due to congenital deficiency of intrinsic factor Finding site Hematopoietic system structure false Inferred relationship Existential restriction modifier (core metadata concept)
Megaloblastic anaemia due to congenital deficiency of intrinsic factor Due to Congenital deficiency of intrinsic factor true Inferred relationship Existential restriction modifier (core metadata concept) 4
Megaloblastic anaemia due to congenital deficiency of intrinsic factor Has interpretation Below reference range true Inferred relationship Existential restriction modifier (core metadata concept) 1
Megaloblastic anaemia due to congenital deficiency of intrinsic factor Has interpretation Below reference range true Inferred relationship Existential restriction modifier (core metadata concept) 2
Megaloblastic anaemia due to congenital deficiency of intrinsic factor Interprets Red blood cell count true Inferred relationship Existential restriction modifier (core metadata concept) 1
Megaloblastic anaemia due to congenital deficiency of intrinsic factor Interprets Measurement of total haemoglobin concentration true Inferred relationship Existential restriction modifier (core metadata concept) 2

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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