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


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

Descriptions:

Id Description Lang Type Status Case? Module
70881014 HNSHA due to hexokinase deficiency en Synonym Active Entire term case sensitive SNOMED CT core module
70882019 Hexokinase deficiency anemia en Synonym Active Entire term case insensitive SNOMED CT core module
493331017 Hexokinase deficiency anaemia en Synonym Active Entire term case insensitive SNOMED CT core module
2620808016 Hereditary nonspherocytic hemolytic anemia (HNSHA) due to hexokinase deficiency en Synonym Active Only initial character case insensitive SNOMED CT core module
2620809012 Hereditary nonspherocytic haemolytic anaemia (HNSHA) due to hexokinase deficiency en Synonym Active Only initial character case insensitive SNOMED CT core module
2913911019 Hereditary nonspherocytic hemolytic anemia due to hexokinase deficiency (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
2914854018 Hereditary nonspherocytic hemolytic anemia due to hexokinase deficiency en Synonym Active Entire term case insensitive SNOMED CT core module
3780592013 Hereditary nonspherocytic haemolytic anaemia due to hexokinase deficiency en Synonym Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hereditary nonspherocytic hemolytic anemia due to hexokinase deficiency Is a Hereditary disorder of hematologic system false Inferred relationship Existential restriction modifier
Hereditary nonspherocytic hemolytic anemia due to hexokinase deficiency Is a Erythrocyte enzyme deficiency true Inferred relationship Existential restriction modifier
Hereditary nonspherocytic hemolytic anemia due to hexokinase deficiency Is a Autosomal hereditary disorder true Inferred relationship Existential restriction modifier
Hereditary nonspherocytic hemolytic anemia due to hexokinase deficiency Is a Congenital anomaly of the hematopoietic system false Inferred relationship Existential restriction modifier
Hereditary nonspherocytic hemolytic anemia due to hexokinase deficiency Is a Anemia due to enzyme deficiency true Inferred relationship Existential restriction modifier
Hereditary nonspherocytic hemolytic anemia due to hexokinase deficiency Is a Inborn error of metabolism true Inferred relationship Existential restriction modifier
Hereditary nonspherocytic hemolytic anemia due to hexokinase deficiency Finding site Erythrocyte true Inferred relationship Existential restriction modifier 5
Hereditary nonspherocytic hemolytic anemia due to hexokinase deficiency Occurrence Congenital true Inferred relationship Existential restriction modifier 4
Hereditary nonspherocytic hemolytic anemia due to hexokinase deficiency Finding site Hematopoietic system structure false Inferred relationship Existential restriction modifier
Hereditary nonspherocytic hemolytic anemia due to hexokinase deficiency Is a Hereditary nonspherocytic hemolytic anemia true Inferred relationship Existential restriction modifier
Hereditary nonspherocytic hemolytic anemia due to hexokinase deficiency Associated etiologic finding Enzymopathy false Inferred relationship Existential restriction modifier
Hereditary nonspherocytic hemolytic anemia due to hexokinase deficiency Is a Hemolytic anemia due to hexokinase deficiency true Inferred relationship Existential restriction modifier
Hereditary nonspherocytic hemolytic anemia due to hexokinase deficiency Associated etiologic finding Deficiency of hexokinase false Inferred relationship Existential restriction modifier
Hereditary nonspherocytic hemolytic anemia due to hexokinase deficiency Has definitional manifestation Erythropenia false Inferred relationship Existential restriction modifier
Hereditary nonspherocytic hemolytic anemia due to hexokinase deficiency Finding site Hematopoietic system structure false Inferred relationship Existential restriction modifier
Hereditary nonspherocytic hemolytic anemia due to hexokinase deficiency Due to Deficiency of hexokinase true Inferred relationship Existential restriction modifier 6
Hereditary nonspherocytic hemolytic anemia due to hexokinase deficiency Is a Congenital anemia true Inferred relationship Existential restriction modifier
Hereditary nonspherocytic hemolytic anemia due to hexokinase deficiency Finding site Body system structure false Inferred relationship Existential restriction modifier
Hereditary nonspherocytic hemolytic anemia due to hexokinase deficiency Has definitional manifestation Hemolysis false Inferred relationship Existential restriction modifier
Hereditary nonspherocytic hemolytic anemia due to hexokinase deficiency Has interpretation Below reference range true Inferred relationship Existential restriction modifier 1
Hereditary nonspherocytic hemolytic anemia due to hexokinase deficiency Has interpretation Below reference range true Inferred relationship Existential restriction modifier 2
Hereditary nonspherocytic hemolytic anemia due to hexokinase deficiency Interprets Red blood cell count true Inferred relationship Existential restriction modifier 1
Hereditary nonspherocytic hemolytic anemia due to hexokinase deficiency Interprets Measurement of total hemoglobin concentration true Inferred relationship Existential restriction modifier 2
Hereditary nonspherocytic hemolytic anemia due to hexokinase deficiency Interprets Erythrocyte destruction, function false Inferred relationship Existential restriction modifier
Hereditary nonspherocytic hemolytic anemia due to hexokinase deficiency Has interpretation Present true Inferred relationship Existential restriction modifier 3
Hereditary nonspherocytic hemolytic anemia due to hexokinase deficiency Interprets Hemolysis true Inferred relationship Existential restriction modifier 3

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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