56205004: Hereditary persistence of fetal hemoglobin, nondeletion type (disorder)

SNOMED CT Concept\Clinical finding\...

\Evaluation finding\Measurement finding\Finding of substance level\Finding of protein level\Hemoglobin finding\Hemoglobin level outside reference range\Hemoglobin below reference range\Anemia due to disturbance of hemoglobin synthesis\Thalassemia\Hereditary persistence of fetal hemoglobin thalassemia\Hereditary persistence of fetal hemoglobin, nondeletion type
\Evaluation finding\Measurement finding\Measurement finding outside reference range\Measurement finding below reference range\Hemoglobin below reference range\Anemia due to disturbance of hemoglobin synthesis\Thalassemia\Hereditary persistence of fetal hemoglobin thalassemia\Hereditary persistence of fetal hemoglobin, nondeletion type
\Evaluation finding\Measurement finding\Measurement finding outside reference range\Hemoglobin level outside reference range\Hemoglobin below reference range\Anemia due to disturbance of hemoglobin synthesis\Thalassemia\Hereditary persistence of fetal hemoglobin thalassemia\Hereditary persistence of fetal hemoglobin, nondeletion type
\Evaluation finding\Hematopoietic system finding\Hematology test outside reference range\Hemoglobin level outside reference range\Hemoglobin below reference range\Anemia due to disturbance of hemoglobin synthesis\Thalassemia\Hereditary persistence of fetal hemoglobin thalassemia\Hereditary persistence of fetal hemoglobin, nondeletion type
\Evaluation finding\Hematopoietic system finding\Hemoglobin finding\Hemoglobin level outside reference range\Hemoglobin below reference range\Anemia due to disturbance of hemoglobin synthesis\Thalassemia\Hereditary persistence of fetal hemoglobin thalassemia\Hereditary persistence of fetal hemoglobin, nondeletion type

\Finding of blood, lymphatics and immune system\Disorder of cellular component of blood\...

\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Thalassemia\Hereditary persistence of fetal hemoglobin thalassemia\Hereditary persistence of fetal hemoglobin, nondeletion type

\Anemia\Anemia due to disturbance of hemoglobin synthesis\Thalassemia\Hereditary persistence of fetal hemoglobin thalassemia\Hereditary persistence of fetal hemoglobin, nondeletion type

\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Thalassemia\Hereditary persistence of fetal hemoglobin thalassemia\Hereditary persistence of fetal hemoglobin, nondeletion type
\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy\Thalassemia\Hereditary persistence of fetal hemoglobin thalassemia\Hereditary persistence of fetal hemoglobin, nondeletion type

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Thalassemia\Hereditary persistence of fetal hemoglobin thalassemia\Hereditary persistence of fetal hemoglobin, nondeletion type
\Disease\Disorder of cellular component of blood\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Thalassemia\Hereditary persistence of fetal hemoglobin thalassemia\Hereditary persistence of fetal hemoglobin, nondeletion type
\Disease\Disorder of cellular component of blood\Anemia\Anemia due to disturbance of hemoglobin synthesis\Thalassemia\Hereditary persistence of fetal hemoglobin thalassemia\Hereditary persistence of fetal hemoglobin, nondeletion type
\Disease\Disorder of cellular component of blood\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Thalassemia\Hereditary persistence of fetal hemoglobin thalassemia\Hereditary persistence of fetal hemoglobin, nondeletion type
\Disease\Disorder of cellular component of blood\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy\Thalassemia\Hereditary persistence of fetal hemoglobin thalassemia\Hereditary persistence of fetal hemoglobin, nondeletion type
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Thalassemia\Hereditary persistence of fetal hemoglobin thalassemia\Hereditary persistence of fetal hemoglobin, nondeletion type
\Disease\Disorder of body system\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Thalassemia\Hereditary persistence of fetal hemoglobin thalassemia\Hereditary persistence of fetal hemoglobin, nondeletion type
\Disease\Disorder of body system\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy\Thalassemia\Hereditary persistence of fetal hemoglobin thalassemia\Hereditary persistence of fetal hemoglobin, nondeletion type
\Disease\Congenital disease\Hereditary hemoglobinopathy\Thalassemia\Hereditary persistence of fetal hemoglobin thalassemia\Hereditary persistence of fetal hemoglobin, nondeletion type

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module

93465016 HPFH nondeletion type en Synonym Active Entire term case sensitive SNOMED CT core module

2621003015 Hereditary persistence of fetal hemoglobin (HPFH) nondeletion type en Synonym Active Only initial character case insensitive SNOMED CT core module

2795474016 Hereditary persistence of foetal haemoglobin (HPFH) nondeletion type en Synonym Active Only initial character case insensitive SNOMED CT core module

2968752016 Hereditary persistence of fetal hemoglobin, nondeletion type en Synonym Active Entire term case insensitive SNOMED CT core module

2968817015 Hereditary persistence of fetal hemoglobin, nondeletion type (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Hereditary persistence of fetal hemoglobin, nondeletion type	Is a	Hereditary persistence of fetal hemoglobin thalassemia	true	Inferred relationship	Existential restriction modifier
Hereditary persistence of fetal hemoglobin, nondeletion type	Finding site	Hematopoietic system structure	false	Inferred relationship	Existential restriction modifier
Hereditary persistence of fetal hemoglobin, nondeletion type	Finding site	Erythrocyte	false	Inferred relationship	Existential restriction modifier
Hereditary persistence of fetal hemoglobin, nondeletion type	Has definitional manifestation	Erythropenia	false	Inferred relationship	Existential restriction modifier
Hereditary persistence of fetal hemoglobin, nondeletion type	Finding site	Hematopoietic system structure	false	Inferred relationship	Existential restriction modifier
Hereditary persistence of fetal hemoglobin, nondeletion type	Finding site	Body system structure	false	Inferred relationship	Existential restriction modifier
Hereditary persistence of fetal hemoglobin, nondeletion type	Has interpretation	Below reference range	false	Inferred relationship	Existential restriction modifier	1
Hereditary persistence of fetal hemoglobin, nondeletion type	Interprets	Measurement of total hemoglobin concentration	false	Inferred relationship	Existential restriction modifier	1
Hereditary persistence of fetal hemoglobin, nondeletion type	Has interpretation	Below reference range	true	Inferred relationship	Existential restriction modifier	2
Hereditary persistence of fetal hemoglobin, nondeletion type	Interprets	Red blood cell count	false	Inferred relationship	Existential restriction modifier	2
Hereditary persistence of fetal hemoglobin, nondeletion type	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	3
Hereditary persistence of fetal hemoglobin, nondeletion type	Finding site	Erythrocyte	true	Inferred relationship	Existential restriction modifier	3
Hereditary persistence of fetal hemoglobin, nondeletion type	Interprets	Measurement of total hemoglobin concentration	true	Inferred relationship	Existential restriction modifier	2

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
93465016	HPFH nondeletion type	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
2621003015	Hereditary persistence of fetal hemoglobin (HPFH) nondeletion type	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
2795474016	Hereditary persistence of foetal haemoglobin (HPFH) nondeletion type	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
2968752016	Hereditary persistence of fetal hemoglobin, nondeletion type	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
2968817015	Hereditary persistence of fetal hemoglobin, nondeletion type (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module