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124331002: Deficiency of pyruvate kinase (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
204066017 Deficiency of phosphoenolpyruvate kinase en Synonym Active Entire term case insensitive SNOMED CT core module
204067014 Deficiency of phosphoenol transphosphorylase en Synonym Active Entire term case insensitive SNOMED CT core module
204068016 Deficiency of pyruvate kinase en Synonym Active Entire term case insensitive SNOMED CT core module
727969017 Deficiency of pyruvate kinase (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
1220694016 PK - Pyruvate kinase deficiency en Synonym Active Entire term case sensitive SNOMED CT core module
1495625017 Pyruvate kinase 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
Deficiency of pyruvate kinase Is a Deficiency of transferase true Inferred relationship Existential restriction modifier
Deficiency of pyruvate kinase Finding site Entire hematological system false Inferred relationship Existential restriction modifier
Deficiency of pyruvate kinase Is a Disorder of body system false Inferred relationship Existential restriction modifier
Inbound Relationships Type Active Source Characteristic Refinability Group
Hereditary nonspherocytic hemolytic anemia due to pyruvate kinase deficiency Is a False Deficiency of pyruvate kinase Inferred relationship Existential restriction modifier
Hemolytic anemia due to pyruvate kinase deficiency Associated etiologic finding False Deficiency of pyruvate kinase Inferred relationship Existential restriction modifier
Hereditary nonspherocytic hemolytic anemia due to pyruvate kinase deficiency Associated etiologic finding False Deficiency of pyruvate kinase Inferred relationship Existential restriction modifier
Hereditary nonspherocytic hemolytic anemia due to pyruvate kinase deficiency Due to True Deficiency of pyruvate kinase Inferred relationship Existential restriction modifier 5
Hemolytic anemia due to pyruvate kinase deficiency Due to False Deficiency of pyruvate kinase Inferred relationship Existential restriction modifier 5
Pyruvate kinase deficiency spot test Has focus False Deficiency of pyruvate kinase Inferred relationship Existential restriction modifier 1
Glycogen storage disease due to muscle pyruvate kinase deficiency Due to True Deficiency of pyruvate kinase Inferred relationship Existential restriction modifier 2
Pyruvate kinase deficiency spot test Has focus True Deficiency of pyruvate kinase Inferred relationship Existential restriction modifier 2
Red blood cell pyruvate kinase screening test Has focus True Deficiency of pyruvate kinase Inferred relationship Existential restriction modifier 3
Red blood cell pyruvate kinase screening test Has focus False Deficiency of pyruvate kinase Inferred relationship Existential restriction modifier 1

This concept is not in any reference sets

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