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74703006: Hereditary nonspherocytic hemolytic anemia due to pyruvate kinase deficiency (disorder)

Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jan 2003. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
124061015 HNSHA due to pyruvate kinase deficiency en Synonym Inactive Entire term case sensitive SNOMED CT core module
124062010 Pyruvate kinase deficiency anemia en Synonym Active Entire term case insensitive SNOMED CT core module
124063017 PK deficiency anemia en Synonym Inactive Entire term case sensitive SNOMED CT core module
200479013 Pyruvate kinase deficiency anaemia en Synonym Active Entire term case insensitive SNOMED CT core module
200480011 PK deficiency anaemia en Synonym Inactive Entire term case sensitive SNOMED CT core module
815232011 HNSHA due to pyruvate kinase deficiency (disorder) en Fully specified name Inactive Entire term case sensitive SNOMED CT core module
2612591017 Hereditary nonspherocytic hemolytic anemia (HNSHA) due to pyruvate kinase deficiency (disorder) en Fully specified name Inactive Only initial character case insensitive SNOMED CT core module
2621111011 Hereditary nonspherocytic hemolytic anemia (HNSHA) due to pyruvate kinase deficiency en Synonym Inactive Only initial character case insensitive SNOMED CT core module
2621112016 Hereditary nonspherocytic haemolytic anaemia (HNSHA) due to pyruvate kinase deficiency en Synonym Inactive Only initial character case insensitive SNOMED CT core module
2913298015 Hereditary nonspherocytic hemolytic anemia due to pyruvate kinase deficiency (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
2913628019 Hereditary nonspherocytic hemolytic anemia due to pyruvate kinase deficiency en Synonym Active Entire term case insensitive SNOMED CT core module
3780591018 Hereditary nonspherocytic haemolytic anaemia due to pyruvate kinase deficiency en Synonym Active Entire term case insensitive SNOMED CT core module
4673191012 PK (pyruvate kinase) deficiency hemolytic anemia en Synonym Active Entire term case sensitive SNOMED CT core module
4673192017 PK (pyruvate kinase) deficiency haemolytic anaemia en Synonym Active Entire term case sensitive SNOMED CT core module
4673715012 HNSHA (hereditary nonspherocytic hemolytic anemia) due to pyruvate kinase deficiency en Synonym Active Entire term case sensitive SNOMED CT core module
4673717016 HNSHA (hereditary nonspherocytic haemolytic anaemia) due to pyruvate kinase deficiency en Synonym Active Entire term case sensitive SNOMED CT core module

0 descendants.

Expanded Value Set

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