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323666000: Anemia due to intrinsic red cell abnormality (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
465061011 Anaemia due to intrinsic red cell abnormality en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
465062016 Anemia due to intrinsic red cell abnormality en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
717606012 Anemia due to intrinsic red cell abnormality (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
465061011 Anaemia due to intrinsic red cell abnormality en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
465061011 Anaemia due to intrinsic red cell abnormality en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
465062016 Anemia due to intrinsic red cell abnormality en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
465062016 Anemia due to intrinsic red cell abnormality en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
717606012 Anemia due to intrinsic red cell abnormality (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
717606012 Anemia due to intrinsic red cell abnormality (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
304081000077116 anémie causée par une anomalie constitutionnelle des érythrocytes fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
304081000077116 anémie causée par une anomalie constitutionnelle des érythrocytes fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

40 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Anaemia due to intrinsic red cell abnormality Is a Anaemia true Inferred relationship Existential restriction modifier (core metadata concept)
Anaemia due to intrinsic red cell abnormality Finding site Hematopoietic system structure false Inferred relationship Existential restriction modifier (core metadata concept)
Anaemia due to intrinsic red cell abnormality Finding site Erythrocyte false Inferred relationship Existential restriction modifier (core metadata concept)
Anaemia due to intrinsic red cell abnormality Finding site Hematopoietic system structure false Inferred relationship Existential restriction modifier (core metadata concept)
Anaemia due to intrinsic red cell abnormality Has definitional manifestation érythropénie false Inferred relationship Existential restriction modifier (core metadata concept)
Anaemia due to intrinsic red cell abnormality Has interpretation Below reference range false Inferred relationship Existential restriction modifier (core metadata concept) 1
Anaemia due to intrinsic red cell abnormality Interprets Measurement of total haemoglobin concentration false Inferred relationship Existential restriction modifier (core metadata concept) 1
Anaemia due to intrinsic red cell abnormality Has interpretation Below reference range false Inferred relationship Existential restriction modifier (core metadata concept) 2
Anaemia due to intrinsic red cell abnormality Interprets Red blood cell count false Inferred relationship Existential restriction modifier (core metadata concept) 2
Inbound Relationships Type Active Source Characteristic Refinability Group
Anemia due to membrane defect (disorder) Is a True Anaemia due to intrinsic red cell abnormality Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary elliptocytosis due to glycophorin C deficiency Is a True Anaemia due to intrinsic red cell abnormality Inferred relationship Existential restriction modifier (core metadata concept)
Paroxysmal nocturnal haemoglobinuria Is a True Anaemia due to intrinsic red cell abnormality Inferred relationship Existential restriction modifier (core metadata concept)
Stomatocytosis (disorder) Is a True Anaemia due to intrinsic red cell abnormality Inferred relationship Existential restriction modifier (core metadata concept)
Rh deficiency syndrome Is a True Anaemia due to intrinsic red cell abnormality Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary elliptocytosis due to deficiency of protein 4.1 Is a True Anaemia due to intrinsic red cell abnormality Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary elliptocytosis due to beta spectrin-ankyrin interaction Is a True Anaemia due to intrinsic red cell abnormality Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary elliptocytosis due to beta spectrin defect in self-association Is a True Anaemia due to intrinsic red cell abnormality Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary elliptocytosis due to abnormal protein 4.1 Is a True Anaemia due to intrinsic red cell abnormality Inferred relationship Existential restriction modifier (core metadata concept)
Xerocytosis Is a True Anaemia due to intrinsic red cell abnormality Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary elliptocytosis due to alpha spectrin defect Is a True Anaemia due to intrinsic red cell abnormality Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary pyropoikilocytosis Is a True Anaemia due to intrinsic red cell abnormality Inferred relationship Existential restriction modifier (core metadata concept)
Hb S disease Is a True Anaemia due to intrinsic red cell abnormality Inferred relationship Existential restriction modifier (core metadata concept)
Erythrogenesis imperfecta Is a False Anaemia due to intrinsic red cell abnormality Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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