FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.4-SNAPSHOT  |  FHIR Version n/a  User: [n/a]

234409003: Erythrocyte membrane 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
351205018 Erythrocyte membrane abnormality en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
622723016 Erythrocyte membrane abnormality (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
351205018 Erythrocyte membrane abnormality en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
351205018 Erythrocyte membrane abnormality en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
622723016 Erythrocyte membrane abnormality (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
622723016 Erythrocyte membrane abnormality (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
6110261000241118 anomalie de la membrane des érythrocytes fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6110271000241114 anomalie de la membrane des globules rouges fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6110281000241111 anomalie membranaire érythrocytaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6110261000241118 anomalie de la membrane des érythrocytes fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6110271000241114 anomalie de la membrane des globules rouges fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6110281000241111 anomalie membranaire érythrocytaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

26 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Erythrocyte membrane abnormality Is a Red blood cell disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Erythrocyte membrane abnormality Finding site Erythrocyte true Inferred relationship Existential restriction modifier (core metadata concept) 1
Erythrocyte membrane abnormality Finding site Hematopoietic system structure false Inferred relationship Existential restriction modifier (core metadata concept)
Erythrocyte membrane abnormality Finding site Hematopoietic system structure false Inferred relationship Existential restriction modifier (core metadata concept)
Erythrocyte membrane abnormality Has definitional manifestation Red blood cell finding (finding) false Inferred relationship Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group
elliptocytose congénitale Is a False Erythrocyte membrane abnormality Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary elliptocytosis Is a True Erythrocyte membrane abnormality Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary elliptocytosis with transient poikilocytosis (disorder) Is a False Erythrocyte membrane abnormality Inferred relationship Existential restriction modifier (core metadata concept)
Blood group deletion syndrome Is a True Erythrocyte membrane abnormality Inferred relationship Existential restriction modifier (core metadata concept)
Abnormal cation transport syndrome Is a True Erythrocyte membrane abnormality Inferred relationship Existential restriction modifier (core metadata concept)
lipoprotéinémie alpha/bêta Is a False Erythrocyte membrane abnormality Inferred relationship Existential restriction modifier (core metadata concept)
Lecithin cholesterol acyltransferase deficiency Is a False Erythrocyte membrane abnormality Inferred relationship Existential restriction modifier (core metadata concept)
March hemoglobinuria Is a False Erythrocyte membrane abnormality Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary acanthocytosis (disorder) Is a True Erythrocyte membrane abnormality Inferred relationship Existential restriction modifier (core metadata concept)
Rh deficiency syndrome Is a True Erythrocyte membrane abnormality Inferred relationship Existential restriction modifier (core metadata concept)
Phosphatidylcholine-sterol acyltransferase deficiency Is a False Erythrocyte membrane abnormality Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary spherocytosis (disorder) Is a True Erythrocyte membrane abnormality Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary pyropoikilocytosis Is a True Erythrocyte membrane abnormality Inferred relationship Existential restriction modifier (core metadata concept)

Reference Sets

Description inactivation indicator reference set

GB English

US English

Back to Start