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363041004: Congenital nonspherocytic hemolytic anemia due to inborn error of metabolism (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
482176016 Congenital nonspherocytic hemolytic anemia due to inborn error of metabolism en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
754820012 Congenital nonspherocytic hemolytic anemia due to inborn error of metabolism (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1206544013 Congenital nonspherocytic haemolytic anaemia due to inborn error of metabolism en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
482176016 Congenital nonspherocytic hemolytic anemia due to inborn error of metabolism en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
482176016 Congenital nonspherocytic hemolytic anemia due to inborn error of metabolism en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
754820012 Congenital nonspherocytic hemolytic anemia due to inborn error of metabolism (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
754820012 Congenital nonspherocytic hemolytic anemia due to inborn error of metabolism (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1206544013 Congenital nonspherocytic haemolytic anaemia due to inborn error of metabolism en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1206544013 Congenital nonspherocytic haemolytic anaemia due to inborn error of metabolism en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5883961000241110 anémie hémolytique congénitale non sphérocytaire due à une erreur innée du métabolisme fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5883971000241119 anémie hémolytique congénitale non sphérocytaire due à une erreur métabolique innée fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5883961000241110 anémie hémolytique congénitale non sphérocytaire due à une erreur innée du métabolisme fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5883971000241119 anémie hémolytique congénitale non sphérocytaire due à une erreur métabolique innée fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital nonspherocytic hemolytic anemia due to inborn error of metabolism (disorder) Is a Inborn error of metabolism true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital nonspherocytic hemolytic anemia due to inborn error of metabolism (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital nonspherocytic hemolytic anemia due to inborn error of metabolism (disorder) Finding site Body system structure false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital nonspherocytic hemolytic anemia due to inborn error of metabolism (disorder) Is a Hereditary nonspherocytic haemolytic anaemia true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital nonspherocytic hemolytic anemia due to inborn error of metabolism (disorder) Is a Hereditary disorder of haematologic sysem false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital nonspherocytic hemolytic anemia due to inborn error of metabolism (disorder) Is a Congenital anomaly of the haematopoietic system false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital nonspherocytic hemolytic anemia due to inborn error of metabolism (disorder) Finding site Erythrocyte false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital nonspherocytic hemolytic anemia due to inborn error of metabolism (disorder) Finding site Hematopoietic system structure false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital nonspherocytic hemolytic anemia due to inborn error of metabolism (disorder) Has definitional manifestation érythropénie false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital nonspherocytic hemolytic anemia due to inborn error of metabolism (disorder) Is a Congenital anemia false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital nonspherocytic hemolytic anemia due to inborn error of metabolism (disorder) Finding site Body system structure false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital nonspherocytic hemolytic anemia due to inborn error of metabolism (disorder) Has definitional manifestation Hemolysis false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital nonspherocytic hemolytic anemia due to inborn error of metabolism (disorder) Has interpretation Below reference range true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital nonspherocytic hemolytic anemia due to inborn error of metabolism (disorder) Has interpretation Below reference range true Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital nonspherocytic hemolytic anemia due to inborn error of metabolism (disorder) Interprets Red blood cell count true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital nonspherocytic hemolytic anemia due to inborn error of metabolism (disorder) Interprets Measurement of total haemoglobin concentration true Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital nonspherocytic hemolytic anemia due to inborn error of metabolism (disorder) Interprets Erythrocyte destruction false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital nonspherocytic hemolytic anemia due to inborn error of metabolism (disorder) Is a Congenital haemolytic anaemia true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital nonspherocytic hemolytic anemia due to inborn error of metabolism (disorder) Finding site Erythrocyte true Inferred relationship Existential restriction modifier (core metadata concept) 3
Congenital nonspherocytic hemolytic anemia due to inborn error of metabolism (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 3
Congenital nonspherocytic hemolytic anemia due to inborn error of metabolism (disorder) Has interpretation Present (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 4
Congenital nonspherocytic hemolytic anemia due to inborn error of metabolism (disorder) Interprets Haemolysis 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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