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124331002: Deficiency of pyruvate kinase (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
204066017 Deficiency of phosphoenolpyruvate kinase en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
204067014 Deficiency of phosphoenol transphosphorylase en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
204068016 Deficiency of pyruvate kinase en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
727969017 Deficiency of pyruvate kinase (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1220694016 PK - Pyruvate kinase deficiency en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
1495625017 Pyruvate kinase deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
204066017 Deficiency of phosphoenolpyruvate kinase en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
204066017 Deficiency of phosphoenolpyruvate kinase en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
204067014 Deficiency of phosphoenol transphosphorylase en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
204067014 Deficiency of phosphoenol transphosphorylase en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
204068016 Deficiency of pyruvate kinase en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
204068016 Deficiency of pyruvate kinase en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
727969017 Deficiency of pyruvate kinase (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
727969017 Deficiency of pyruvate kinase (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1220694016 PK - Pyruvate kinase deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1220694016 PK - Pyruvate kinase deficiency en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
1495625017 Pyruvate kinase deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1495625017 Pyruvate kinase deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4772441000241111 déficit en pyruvate kinase fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
4772441000241111 déficit en pyruvate kinase 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
Deficiency of pyruvate kinase Is a Deficiency of transferase true Inferred relationship Existential restriction modifier (core metadata concept)
Deficiency of pyruvate kinase Finding site Entire hematological system (body structure) false Inferred relationship Existential restriction modifier (core metadata concept)
Deficiency of pyruvate kinase Is a Disorder of body system false Inferred relationship Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group
HNSHA (hereditary nonspherocytic hemolytic anemia) due to pyruvate kinase deficiency Is a False Deficiency of pyruvate kinase Inferred relationship Existential restriction modifier (core metadata concept)
Hämolytische Anämie durch Mangel der erythrozytären Pyruvatkinase Associated etiologic finding False Deficiency of pyruvate kinase Inferred relationship Existential restriction modifier (core metadata concept)
HNSHA (hereditary nonspherocytic hemolytic anemia) due to pyruvate kinase deficiency Associated etiologic finding False Deficiency of pyruvate kinase Inferred relationship Existential restriction modifier (core metadata concept)
HNSHA (hereditary nonspherocytic hemolytic anemia) due to pyruvate kinase deficiency Due to True Deficiency of pyruvate kinase Inferred relationship Existential restriction modifier (core metadata concept) 5
Hämolytische Anämie durch Mangel der erythrozytären Pyruvatkinase Due to False Deficiency of pyruvate kinase Inferred relationship Existential restriction modifier (core metadata concept) 5
Pyruvate kinase deficiency spot test Has focus False Deficiency of pyruvate kinase Inferred relationship Existential restriction modifier (core metadata concept) 1
Glycogen storage disease due to muscle pyruvate kinase deficiency Due to True Deficiency of pyruvate kinase Inferred relationship Existential restriction modifier (core metadata concept) 2
Pyruvate kinase deficiency spot test Has focus True Deficiency of pyruvate kinase Inferred relationship Existential restriction modifier (core metadata concept) 2

This concept is not in any reference sets

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