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62268000: Hereditary nonspherocytic hemolytic anemia due to diphosphoglycerate mutase deficiency (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
103490017 HNSHA due to diphosphoglycerate mutase deficiency en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
2621004014 Hereditary nonspherocytic hemolytic anemia (HNSHA) due to diphosphoglycerate mutase deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2621005010 Hereditary nonspherocytic haemolytic anaemia (HNSHA) due to diphosphoglycerate mutase deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2913737012 Hereditary nonspherocytic hemolytic anemia due to diphosphoglycerate mutase deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2914465016 Hereditary nonspherocytic hemolytic anemia due to diphosphoglycerate mutase deficiency (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3780588018 Hereditary nonspherocytic haemolytic anaemia due to diphosphoglycerate mutase deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
HNSHA due to diphosphoglycerate mutase deficiency a pour interprétation (attribut) présent (valeur de l'attribut) true Inferred relationship Some 3
HNSHA due to diphosphoglycerate mutase deficiency interprète (attribut) Hemolysis (observable entity) true Inferred relationship Some 3
HNSHA due to diphosphoglycerate mutase deficiency est un(e) (attribut) Deficiency of bisphosphoglycerate mutase false Inferred relationship Some
HNSHA due to diphosphoglycerate mutase deficiency est un(e) (attribut) Hereditary nonspherocytic haemolytic anaemia true Inferred relationship Some
HNSHA due to diphosphoglycerate mutase deficiency Associated aetiologic finding Enzymopathy false Inferred relationship Some
HNSHA due to diphosphoglycerate mutase deficiency Associated aetiologic finding Deficiency of bisphosphoglycerate mutase false Inferred relationship Some
HNSHA due to diphosphoglycerate mutase deficiency localisation d'une constatation (attribut) structure du système hématopoïétique false Inferred relationship Some
HNSHA due to diphosphoglycerate mutase deficiency est défini par la manifestation de (attribut) Erythropenia false Inferred relationship Some
HNSHA due to diphosphoglycerate mutase deficiency est un(e) (attribut) Autosomal recessive hereditary disorder true Inferred relationship Some
HNSHA due to diphosphoglycerate mutase deficiency est un(e) (attribut) Erythrocyte enzyme deficiency true Inferred relationship Some
HNSHA due to diphosphoglycerate mutase deficiency est un(e) (attribut) Hereditary disorder of hematologic system false Inferred relationship Some
HNSHA due to diphosphoglycerate mutase deficiency est un(e) (attribut) Anemia due to enzyme deficiency true Inferred relationship Some
HNSHA due to diphosphoglycerate mutase deficiency est un(e) (attribut) anomalie congénitale du système hématopoïétique false Inferred relationship Some
HNSHA due to diphosphoglycerate mutase deficiency est un(e) (attribut) Inborn error of metabolism false Inferred relationship Some
HNSHA due to diphosphoglycerate mutase deficiency Due to Deficiency of bisphosphoglycerate mutase true Inferred relationship Some 5
HNSHA due to diphosphoglycerate mutase deficiency est défini par la manifestation de (attribut) Hemolysis false Inferred relationship Some
HNSHA due to diphosphoglycerate mutase deficiency localisation d'une constatation (attribut) structure d'un système corporel false Inferred relationship Some
HNSHA due to diphosphoglycerate mutase deficiency a pour interprétation (attribut) au-dessous de l'étendue de référence true Inferred relationship Some 1
HNSHA due to diphosphoglycerate mutase deficiency interprète (attribut) Red blood cell count true Inferred relationship Some 1
HNSHA due to diphosphoglycerate mutase deficiency a pour interprétation (attribut) au-dessous de l'étendue de référence true Inferred relationship Some 2
HNSHA due to diphosphoglycerate mutase deficiency interprète (attribut) Measurement of total haemoglobin concentration true Inferred relationship Some 2
HNSHA due to diphosphoglycerate mutase deficiency localisation d'une constatation (attribut) Erythrocyte true Inferred relationship Some 4
HNSHA due to diphosphoglycerate mutase deficiency localisation d'une constatation (attribut) structure du système hématopoïétique false Inferred relationship Some
HNSHA due to diphosphoglycerate mutase deficiency survenue (attribut) congénital false Inferred relationship Some
HNSHA due to diphosphoglycerate mutase deficiency interprète (attribut) Erythrocyte destruction, function (observable entity) false Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Client's clinical problems, conditions, diagnoses, symptoms, findings, complaints reference set (foundation metadata concept)

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