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59644002: Hereditary nonspherocytic hemolytic anemia due to phosphoglycerate kinase deficiency (disorder)


Status: current, Defined. Date: 31-Jan 2003. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
198909017 HNSHA due to phosphoglycerate kinase deficiency en Synonym Active Case sensitive SNOMED CT core
2620982017 Hereditary nonspherocytic hemolytic anemia (HNSHA) due to phosphoglycerate kinase deficiency en Synonym Active Initial character case insensitive SNOMED CT core
2620983010 Hereditary nonspherocytic haemolytic anaemia (HNSHA) due to phosphoglycerate kinase deficiency en Synonym Active Initial character case insensitive SNOMED CT core
2913263018 Hereditary nonspherocytic hemolytic anemia due to phosphoglycerate kinase deficiency en Synonym Active Case insensitive SNOMED CT core
2915032010 Hereditary nonspherocytic hemolytic anemia due to phosphoglycerate kinase deficiency (disorder) en Fully specified name Active Case insensitive SNOMED CT core
3780593015 Hereditary nonspherocytic haemolytic anaemia due to phosphoglycerate kinase deficiency en Synonym Active Case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
HNSHA due to phosphoglycerate kinase deficiency Has interpretation Present true Inferred relationship Some 3
HNSHA due to phosphoglycerate kinase deficiency Interprets Haemolysis true Inferred relationship Some 3
HNSHA due to phosphoglycerate kinase deficiency Is a Hereditary nonspherocytic haemolytic anaemia true Inferred relationship Some
HNSHA due to phosphoglycerate kinase deficiency Associated etiologic finding Enzymopathy false Inferred relationship Some
HNSHA due to phosphoglycerate kinase deficiency Associated etiologic finding Deficiency of phosphoglycerate kinase false Inferred relationship Some
HNSHA due to phosphoglycerate kinase deficiency Finding site Haematopoietic system structure false Inferred relationship Some
HNSHA due to phosphoglycerate kinase deficiency Has definitional manifestation Erythropenia false Inferred relationship Some
HNSHA due to phosphoglycerate kinase deficiency Is a Congenital anomaly of the haematopoietic system false Inferred relationship Some
HNSHA due to phosphoglycerate kinase deficiency Is a Anaemia due to enzyme deficiency true Inferred relationship Some
HNSHA due to phosphoglycerate kinase deficiency Is a Inborn error of metabolism false Inferred relationship Some
HNSHA due to phosphoglycerate kinase deficiency Is a Erythrocyte enzyme deficiency true Inferred relationship Some
HNSHA due to phosphoglycerate kinase deficiency Is a Hereditary disorder of haematologic system false Inferred relationship Some
HNSHA due to phosphoglycerate kinase deficiency Due to Deficiency of phosphoglycerate kinase true Inferred relationship Some 5
HNSHA due to phosphoglycerate kinase deficiency Finding site Body system structure false Inferred relationship Some
HNSHA due to phosphoglycerate kinase deficiency Has definitional manifestation Haemolysis false Inferred relationship Some
HNSHA due to phosphoglycerate kinase deficiency Has interpretation Below reference range true Inferred relationship Some 1
HNSHA due to phosphoglycerate kinase deficiency Interprets Red blood cell count true Inferred relationship Some 1
HNSHA due to phosphoglycerate kinase deficiency Has interpretation Below reference range true Inferred relationship Some 2
HNSHA due to phosphoglycerate kinase deficiency Interprets Measurement of total haemoglobin concentration true Inferred relationship Some 2
HNSHA due to phosphoglycerate kinase deficiency Finding site Erythrocyte true Inferred relationship Some 4
HNSHA due to phosphoglycerate kinase deficiency Interprets Nutritional deficiency false Inferred relationship Some
HNSHA due to phosphoglycerate kinase deficiency Occurrence Congenital false Inferred relationship Some
HNSHA due to phosphoglycerate kinase deficiency Finding site Haematopoietic system structure false Inferred relationship Some
HNSHA due to phosphoglycerate kinase deficiency Interprets Erythrocyte destruction false Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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