FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.10  |  FHIR Version n/a  User: [n/a]

323666000: Anemia due to intrinsic red cell abnormality (disorder)

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

Descriptions:

Id Description Lang Type Status Case? Module
465061011 Anaemia due to intrinsic red cell abnormality en Synonym Active Entire term case insensitive SNOMED CT core module
465062016 Anemia due to intrinsic red cell abnormality en Synonym Active Entire term case insensitive SNOMED CT core module
717606012 Anemia due to intrinsic red cell abnormality (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

40 descendants. Search Descendants:

Expanded Value Set

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

This concept is not in any reference sets

Back to Start