127065001: Familial erythrocytosis due to diphosphoglycerate mutase deficiency (disorder)

• SNOMED CT Concept\constatation clinique\...
• \Evaluation finding\Finding of cellular component of blood (finding)\constatation à propos de la lignée rouge\Erythrocytosis\Familial erythrocytosis\Familial erythrocytosis due to diphosphoglycerate mutase deficiency
• \Evaluation finding\Measurement finding\Measurement finding outside reference range\Abnormal blood cell count\RBC count abnormal\Red blood cell count raised (finding)\Erythrocytosis\Familial erythrocytosis\Familial erythrocytosis due to diphosphoglycerate mutase deficiency
• \Evaluation finding\Measurement finding\Measurement finding outside reference range\Measurement finding above reference range\Red blood cell count raised (finding)\Erythrocytosis\Familial erythrocytosis\Familial erythrocytosis due to diphosphoglycerate mutase deficiency
• \Evaluation finding\Measurement finding\Red blood cell count - finding\RBC count abnormal\Red blood cell count raised (finding)\Erythrocytosis\Familial erythrocytosis\Familial erythrocytosis due to diphosphoglycerate mutase deficiency
• \Evaluation finding\Hematopoietic system finding\constatation à propos de la lignée rouge\Erythrocytosis\Familial erythrocytosis\Familial erythrocytosis due to diphosphoglycerate mutase deficiency
• \constatation à propos du sang, des lymphatiques et du système immunitaire\anomalie des éléments figurés du sang (trouble)\...
• \troubles héréditaires des éléments figurés du sang\Hereditary red blood cell disorder (disorder)\Familial erythrocytosis\Familial erythrocytosis due to diphosphoglycerate mutase deficiency
• \anomalie de la lignée rouge\Hereditary red blood cell disorder (disorder)\Familial erythrocytosis\Familial erythrocytosis due to diphosphoglycerate mutase deficiency
• \anomalie de la lignée rouge\Erythrocytosis\Familial erythrocytosis\Familial erythrocytosis due to diphosphoglycerate mutase deficiency
• \Disease\Genetic disease\maladie héréditaire\Hereditary disorder by system\troubles héréditaires des éléments figurés du sang\Hereditary red blood cell disorder (disorder)\Familial erythrocytosis\Familial erythrocytosis due to diphosphoglycerate mutase deficiency
• \Disease\Genetic disease\maladie héréditaire\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Familial erythrocytosis due to diphosphoglycerate mutase deficiency
• \Disease\anomalie des éléments figurés du sang (trouble)\troubles héréditaires des éléments figurés du sang\Hereditary red blood cell disorder (disorder)\Familial erythrocytosis\Familial erythrocytosis due to diphosphoglycerate mutase deficiency
• \Disease\anomalie des éléments figurés du sang (trouble)\anomalie de la lignée rouge\Hereditary red blood cell disorder (disorder)\Familial erythrocytosis\Familial erythrocytosis due to diphosphoglycerate mutase deficiency
• \Disease\anomalie des éléments figurés du sang (trouble)\anomalie de la lignée rouge\Erythrocytosis\Familial erythrocytosis\Familial erythrocytosis due to diphosphoglycerate mutase deficiency
• \Disease\affection d'un système corporel\Hereditary disorder by system\troubles héréditaires des éléments figurés du sang\Hereditary red blood cell disorder (disorder)\Familial erythrocytosis\Familial erythrocytosis due to diphosphoglycerate mutase deficiency
• \Disease\affection d'un système corporel\anomalie de la lignée rouge\Hereditary red blood cell disorder (disorder)\Familial erythrocytosis\Familial erythrocytosis due to diphosphoglycerate mutase deficiency
• \Disease\affection d'un système corporel\anomalie de la lignée rouge\Erythrocytosis\Familial erythrocytosis\Familial erythrocytosis due to diphosphoglycerate mutase deficiency

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
353012	Familial erythrocytosis due to diphosphoglycerate mutase deficiency	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
731107016	Familial erythrocytosis due to diphosphoglycerate mutase deficiency (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core

Expanded Value Set

This concept is not in any reference sets

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