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75443009: Hereditary elliptocytosis due to abnormal protein 4.1 (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
125306014 Hereditary elliptocytosis due to abnormal protein 4.1 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
816053017 Hereditary elliptocytosis due to abnormal protein 4.1 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
125306014 Hereditary elliptocytosis due to abnormal protein 4.1 en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
125306014 Hereditary elliptocytosis due to abnormal protein 4.1 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
816053017 Hereditary elliptocytosis due to abnormal protein 4.1 (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
816053017 Hereditary elliptocytosis due to abnormal protein 4.1 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
6290491000241110 elliptocytose héréditaire due à une anomalie de la protéine 4.1 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6290501000241115 EH (elliptocytose héréditaire) due à une anomalie de la protéine 4.1 fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6290491000241110 elliptocytose héréditaire due à une anomalie de la protéine 4.1 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6290501000241115 EH (elliptocytose héréditaire) due à une anomalie de la protéine 4.1 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 abnormal protein 4.1 Is a Anaemia due to intrinsic red cell abnormality true Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary elliptocytosis due to abnormal protein 4.1 Is a Hereditary elliptocytosis true Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary elliptocytosis due to abnormal protein 4.1 Is a Hereditary disorder of haematologic sysem false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary elliptocytosis due to abnormal protein 4.1 Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary elliptocytosis due to abnormal protein 4.1 Finding site Hematopoietic system structure false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary elliptocytosis due to abnormal protein 4.1 Finding site Erythrocyte false Inferred relationship Existential restriction modifier (core metadata concept) 3
Hereditary elliptocytosis due to abnormal protein 4.1 Has definitional manifestation érythropénie false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary elliptocytosis due to abnormal protein 4.1 Finding site Hematopoietic system structure false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary elliptocytosis due to abnormal protein 4.1 Finding site Body system structure false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary elliptocytosis due to abnormal protein 4.1 Has interpretation Below reference range true Inferred relationship Existential restriction modifier (core metadata concept) 1
Hereditary elliptocytosis due to abnormal protein 4.1 Interprets Measurement of total haemoglobin concentration true Inferred relationship Existential restriction modifier (core metadata concept) 1
Hereditary elliptocytosis due to abnormal protein 4.1 Has interpretation Below reference range true Inferred relationship Existential restriction modifier (core metadata concept) 2
Hereditary elliptocytosis due to abnormal protein 4.1 Interprets Red blood cell count true Inferred relationship Existential restriction modifier (core metadata concept) 2
Hereditary elliptocytosis due to abnormal protein 4.1 Interprets Haemolysis true Inferred relationship Existential restriction modifier (core metadata concept) 3
Hereditary elliptocytosis due to abnormal protein 4.1 Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 4
Hereditary elliptocytosis due to abnormal protein 4.1 Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 4
Hereditary elliptocytosis due to abnormal protein 4.1 Associated morphology Elliptocyte (cell) true Inferred relationship Existential restriction modifier (core metadata concept) 4
Hereditary elliptocytosis due to abnormal protein 4.1 Has interpretation Present (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 3
Hereditary elliptocytosis due to abnormal protein 4.1 Finding site Erythrocyte 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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