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42484009: Hereditary nonspherocytic hemolytic anemia due to hexokinase deficiency (disorder)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2005. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
70881014 HNSHA due to hexokinase deficiency en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
70882019 Hexokinase deficiency anemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
493331017 Hexokinase deficiency anaemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2620808016 Hereditary nonspherocytic hemolytic anemia (HNSHA) due to hexokinase deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2620809012 Hereditary nonspherocytic haemolytic anaemia (HNSHA) due to hexokinase deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2913911019 Hereditary nonspherocytic hemolytic anemia due to hexokinase deficiency (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2914854018 Hereditary nonspherocytic hemolytic anemia due to hexokinase deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3780592013 Hereditary nonspherocytic haemolytic anaemia due to hexokinase deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
70881014 HNSHA due to hexokinase deficiency en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
70882019 Hexokinase deficiency anemia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
70882019 Hexokinase deficiency anemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
493331017 Hexokinase deficiency anaemia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
493331017 Hexokinase deficiency anaemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
779388011 HNSHA due to hexokinase deficiency (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
779388011 HNSHA due to hexokinase deficiency (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
2612393015 Hereditary nonspherocytic hemolytic anemia (HNSHA) due to hexokinase deficiency (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2620808016 Hereditary nonspherocytic hemolytic anemia (HNSHA) due to hexokinase deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2620809012 Hereditary nonspherocytic haemolytic anaemia (HNSHA) due to hexokinase deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2913911019 Hereditary nonspherocytic hemolytic anemia due to hexokinase deficiency (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2913911019 Hereditary nonspherocytic hemolytic anemia due to hexokinase deficiency (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2914854018 Hereditary nonspherocytic hemolytic anemia due to hexokinase deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2914854018 Hereditary nonspherocytic hemolytic anemia due to hexokinase deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3780592013 Hereditary nonspherocytic haemolytic anaemia due to hexokinase deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
6290161000241110 anémie hémolytique héréditaire non sphérocytaire due à un déficit en hexokinase fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6290161000241110 anémie hémolytique héréditaire non sphérocytaire due à un déficit en hexokinase 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
HNSHA due to hexokinase deficiency Is a Hereditary disorder of haematologic sysem false Inferred relationship Existential restriction modifier (core metadata concept)
HNSHA due to hexokinase deficiency Is a Erythrocyte enzyme deficiency true Inferred relationship Existential restriction modifier (core metadata concept)
HNSHA due to hexokinase deficiency Is a Autosomal hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
HNSHA due to hexokinase deficiency Is a Congenital anomaly of the haematopoietic system false Inferred relationship Existential restriction modifier (core metadata concept)
HNSHA due to hexokinase deficiency Is a Anemia due to enzyme deficiency true Inferred relationship Existential restriction modifier (core metadata concept)
HNSHA due to hexokinase deficiency Is a Inborn error of metabolism true Inferred relationship Existential restriction modifier (core metadata concept)
HNSHA due to hexokinase deficiency Finding site Erythrocyte true Inferred relationship Existential restriction modifier (core metadata concept) 5
HNSHA due to hexokinase deficiency Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 4
HNSHA due to hexokinase deficiency Finding site Hematopoietic system structure false Inferred relationship Existential restriction modifier (core metadata concept)
HNSHA due to hexokinase deficiency Is a Hereditary nonspherocytic haemolytic anaemia true Inferred relationship Existential restriction modifier (core metadata concept)
HNSHA due to hexokinase deficiency Associated etiologic finding Enzymopathy false Inferred relationship Existential restriction modifier (core metadata concept)
HNSHA due to hexokinase deficiency Is a Hemolytic anemia due to hexokinase deficiency true Inferred relationship Existential restriction modifier (core metadata concept)
HNSHA due to hexokinase deficiency Associated etiologic finding Deficiency of hexokinase (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
HNSHA due to hexokinase deficiency Has definitional manifestation érythropénie false Inferred relationship Existential restriction modifier (core metadata concept)
HNSHA due to hexokinase deficiency Finding site Hematopoietic system structure false Inferred relationship Existential restriction modifier (core metadata concept)
HNSHA due to hexokinase deficiency Due to Deficiency of hexokinase (disorder) true Inferred relationship Existential restriction modifier (core metadata concept) 6
HNSHA due to hexokinase deficiency Is a Congenital anemia true Inferred relationship Existential restriction modifier (core metadata concept)
HNSHA due to hexokinase deficiency Finding site Body system structure false Inferred relationship Existential restriction modifier (core metadata concept)
HNSHA due to hexokinase deficiency Has definitional manifestation Hemolysis false Inferred relationship Existential restriction modifier (core metadata concept)
HNSHA due to hexokinase deficiency Has interpretation Below reference range true Inferred relationship Existential restriction modifier (core metadata concept) 1
HNSHA due to hexokinase deficiency Has interpretation Below reference range true Inferred relationship Existential restriction modifier (core metadata concept) 2
HNSHA due to hexokinase deficiency Interprets Red blood cell count true Inferred relationship Existential restriction modifier (core metadata concept) 1
HNSHA due to hexokinase deficiency Interprets Measurement of total haemoglobin concentration true Inferred relationship Existential restriction modifier (core metadata concept) 2
HNSHA due to hexokinase deficiency Interprets Erythrocyte destruction false Inferred relationship Existential restriction modifier (core metadata concept)
HNSHA due to hexokinase deficiency Has interpretation Present (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 3
HNSHA due to hexokinase deficiency Interprets Haemolysis true Inferred relationship Existential restriction modifier (core metadata concept) 3
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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