234353009: Congenital transferrin deficiency (disorder)

SNOMED CT Concept\constatation clinique\...

\Evaluation finding\Microscopic specimen observation (finding)\Microcytosis, red cells (finding)\anémie microcytaire\Congenital transferrin deficiency
\Evaluation finding\Measurement finding\Finding of substance level (finding)\Protein level - finding\Hemoglobin level outside reference range (finding)\Hemoglobin low\anémie microcytaire\Congenital transferrin deficiency
\Evaluation finding\Measurement finding\Finding of substance level (finding)\Protein level - finding\Hemoglobin level outside reference range (finding)\Hemoglobin low\Congenital anemia\Congenital transferrin deficiency
\Evaluation finding\Measurement finding\Finding of substance level (finding)\Protein level - finding\Hemoglobin level outside reference range (finding)\Hemoglobin low\Anemia due to disturbance of hemoglobin synthesis\Congenital transferrin deficiency
\Evaluation finding\Measurement finding\Measurement finding outside reference range\Abnormal blood cell count\RBC count abnormal\numération des globules rouges basse (constatation)\anémie microcytaire\Congenital transferrin deficiency
\Evaluation finding\Measurement finding\Measurement finding outside reference range\Abnormal blood cell count\RBC count abnormal\numération des globules rouges basse (constatation)\Congenital anemia\Congenital transferrin deficiency
\Evaluation finding\Measurement finding\Measurement finding outside reference range\Abnormal blood cell count\cytopénie (constatation)\numération des globules rouges basse (constatation)\anémie microcytaire\Congenital transferrin deficiency
\Evaluation finding\Measurement finding\Measurement finding outside reference range\Abnormal blood cell count\cytopénie (constatation)\numération des globules rouges basse (constatation)\Congenital anemia\Congenital transferrin deficiency
\Evaluation finding\Measurement finding\Measurement finding outside reference range\Measurement finding below reference range (finding)\Hemoglobin low\anémie microcytaire\Congenital transferrin deficiency
\Evaluation finding\Measurement finding\Measurement finding outside reference range\Measurement finding below reference range (finding)\Hemoglobin low\Congenital anemia\Congenital transferrin deficiency
\Evaluation finding\Measurement finding\Measurement finding outside reference range\Measurement finding below reference range (finding)\Hemoglobin low\Anemia due to disturbance of hemoglobin synthesis\Congenital transferrin deficiency
\Evaluation finding\Measurement finding\Measurement finding outside reference range\Measurement finding below reference range (finding)\cytopénie (constatation)\numération des globules rouges basse (constatation)\anémie microcytaire\Congenital transferrin deficiency
\Evaluation finding\Measurement finding\Measurement finding outside reference range\Measurement finding below reference range (finding)\cytopénie (constatation)\numération des globules rouges basse (constatation)\Congenital anemia\Congenital transferrin deficiency
\Evaluation finding\Measurement finding\Measurement finding outside reference range\Hemoglobin level outside reference range (finding)\Hemoglobin low\anémie microcytaire\Congenital transferrin deficiency
\Evaluation finding\Measurement finding\Measurement finding outside reference range\Hemoglobin level outside reference range (finding)\Hemoglobin low\Congenital anemia\Congenital transferrin deficiency
\Evaluation finding\Measurement finding\Measurement finding outside reference range\Hemoglobin level outside reference range (finding)\Hemoglobin low\Anemia due to disturbance of hemoglobin synthesis\Congenital transferrin deficiency
\Evaluation finding\Measurement finding\Red blood cell count - finding\RBC count abnormal\numération des globules rouges basse (constatation)\anémie microcytaire\Congenital transferrin deficiency
\Evaluation finding\Measurement finding\Red blood cell count - finding\RBC count abnormal\numération des globules rouges basse (constatation)\Congenital anemia\Congenital transferrin deficiency
\Evaluation finding\Hematopoietic system finding\Hemoglobin level outside reference range (finding)\Hemoglobin low\anémie microcytaire\Congenital transferrin deficiency
\Evaluation finding\Hematopoietic system finding\Hemoglobin level outside reference range (finding)\Hemoglobin low\Congenital anemia\Congenital transferrin deficiency
\Evaluation finding\Hematopoietic system finding\Hemoglobin level outside reference range (finding)\Hemoglobin low\Anemia due to disturbance of hemoglobin synthesis\Congenital transferrin deficiency
\Evaluation finding\Hematopoietic system finding\Microcytosis, red cells (finding)\anémie microcytaire\Congenital transferrin deficiency

\constatation à propos du sang, des lymphatiques et du système immunitaire\anomalie des éléments figurés du sang (trouble)\anémie\...

\anémie microcytaire\Congenital transferrin deficiency

\Congenital anemia\Congenital transferrin deficiency

\Anemia due to disturbance of hemoglobin synthesis\Congenital transferrin deficiency

\Disease\Genetic disease\maladie héréditaire\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Congenital transferrin deficiency
\Disease\anomalie des éléments figurés du sang (trouble)\anémie\anémie microcytaire\Congenital transferrin deficiency
\Disease\anomalie des éléments figurés du sang (trouble)\anémie\Congenital anemia\Congenital transferrin deficiency
\Disease\anomalie des éléments figurés du sang (trouble)\anémie\Anemia due to disturbance of hemoglobin synthesis\Congenital transferrin deficiency
\Disease\Congenital disease\Congenital anemia\Congenital transferrin 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

351093011 Congenital transferrin deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

622660011 Congenital transferrin deficiency (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Congenital transferrin deficiency	est défini par la manifestation de (attribut)	Erythropenia	false	Inferred relationship	Some
Congenital transferrin deficiency	est défini par la manifestation de (attribut)	Microcytosis, red cells (finding)	false	Inferred relationship	Some
Congenital transferrin deficiency	localisation d'une constatation (attribut)	structure du système hématopoïétique	false	Inferred relationship	Some
Congenital transferrin deficiency	est un(e) (attribut)	anomalie congénitale du système hématopoïétique	false	Inferred relationship	Some
Congenital transferrin deficiency	survenue (attribut)	congénital	true	Inferred relationship	Some	3
Congenital transferrin deficiency	est un(e) (attribut)	Congenital anemia	true	Inferred relationship	Some
Congenital transferrin deficiency	est un(e) (attribut)	anémie microcytaire	true	Inferred relationship	Some
Congenital transferrin deficiency	localisation d'une constatation (attribut)	Erythrocyte	false	Inferred relationship	Some
Congenital transferrin deficiency	localisation d'une constatation (attribut)	structure du système hématopoïétique	false	Inferred relationship	Some
Congenital transferrin deficiency	est un(e) (attribut)	Anemia due to disturbance of hemoglobin synthesis	true	Inferred relationship	Some
Congenital transferrin deficiency	est un(e) (attribut)	Autosomal recessive hereditary disorder	true	Inferred relationship	Some
Congenital transferrin deficiency	est un(e) (attribut)	Hereditary red blood cell disorder (disorder)	false	Inferred relationship	Some
Congenital transferrin deficiency	est un(e) (attribut)	Congenital disease	false	Inferred relationship	Some
Congenital transferrin deficiency	a pour interprétation (attribut)	au-dessous de l'étendue de référence	true	Inferred relationship	Some	1
Congenital transferrin deficiency	a pour interprétation (attribut)	au-dessous de l'étendue de référence	true	Inferred relationship	Some	2
Congenital transferrin deficiency	interprète (attribut)	Red blood cell count	true	Inferred relationship	Some	1
Congenital transferrin deficiency	interprète (attribut)	Measurement of total haemoglobin concentration	true	Inferred relationship	Some	2
Congenital transferrin deficiency	interprète (attribut)	Red blood cell size determination	true	Inferred relationship	Some	4

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
atransferrinémie congénitale	est un(e) (attribut)	True	Congenital transferrin deficiency	Inferred relationship	Some

Reference Sets

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

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Id	Description	Lang	Type	Status	Case?	Module
351093011	Congenital transferrin deficiency	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
622660011	Congenital transferrin deficiency (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core