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66262001: Hereditary elliptocytosis due to beta spectrin-ankyrin interaction (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
110049019 Hereditary elliptocytosis due to beta spectrin-ankyrin interaction en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
805856011 Hereditary elliptocytosis due to beta spectrin-ankyrin interaction (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
110049019 Hereditary elliptocytosis due to beta spectrin-ankyrin interaction en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
110049019 Hereditary elliptocytosis due to beta spectrin-ankyrin interaction en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
805856011 Hereditary elliptocytosis due to beta spectrin-ankyrin interaction (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
805856011 Hereditary elliptocytosis due to beta spectrin-ankyrin interaction (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
6240541000241111 elliptocytose héréditaire due à l'interaction de la spectrine bêta avec l'ankyrine fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6240551000241114 EH (elliptocytose héréditaire) due à l'interaction de la spectrine bêta avec l'ankyrine fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6240541000241111 elliptocytose héréditaire due à l'interaction de la spectrine bêta avec l'ankyrine fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6240551000241114 EH (elliptocytose héréditaire) due à l'interaction de la spectrine bêta avec l'ankyrine fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hereditary elliptocytosis due to beta spectrin-ankyrin interaction Is a Hereditary elliptocytosis true Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary elliptocytosis due to beta spectrin-ankyrin interaction Is a Anaemia due to intrinsic red cell abnormality true Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary elliptocytosis due to beta spectrin-ankyrin interaction Finding site Hematopoietic system structure false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary elliptocytosis due to beta spectrin-ankyrin interaction Finding site Erythrocyte false Inferred relationship Existential restriction modifier (core metadata concept) 3
Hereditary elliptocytosis due to beta spectrin-ankyrin interaction Has definitional manifestation érythropénie false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary elliptocytosis due to beta spectrin-ankyrin interaction Finding site Hematopoietic system structure false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary elliptocytosis due to beta spectrin-ankyrin interaction Finding site Body system structure false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary elliptocytosis due to beta spectrin-ankyrin interaction Has interpretation Below reference range true Inferred relationship Existential restriction modifier (core metadata concept) 1
Hereditary elliptocytosis due to beta spectrin-ankyrin interaction Interprets Measurement of total haemoglobin concentration true Inferred relationship Existential restriction modifier (core metadata concept) 1
Hereditary elliptocytosis due to beta spectrin-ankyrin interaction Has interpretation Below reference range true Inferred relationship Existential restriction modifier (core metadata concept) 2
Hereditary elliptocytosis due to beta spectrin-ankyrin interaction Interprets Red blood cell count true Inferred relationship Existential restriction modifier (core metadata concept) 2
Hereditary elliptocytosis due to beta spectrin-ankyrin interaction Has interpretation Present (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 3
Hereditary elliptocytosis due to beta spectrin-ankyrin interaction Interprets Haemolysis true Inferred relationship Existential restriction modifier (core metadata concept) 3
Hereditary elliptocytosis due to beta spectrin-ankyrin interaction Finding site Erythrocyte true Inferred relationship Existential restriction modifier (core metadata concept) 4
Hereditary elliptocytosis due to beta spectrin-ankyrin interaction Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 4
Hereditary elliptocytosis due to beta spectrin-ankyrin interaction Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 4
Hereditary elliptocytosis due to beta spectrin-ankyrin interaction Associated morphology Elliptocyte (cell) true Inferred relationship Existential restriction modifier (core metadata concept) 4

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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