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9434008: Hereditary pyropoikilocytosis (disorder)

SNOMED CT Concept\Clinical finding\...

\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 pyropoikilocytosis

\Anemia\Anemia due to intrinsic red cell abnormality\Hereditary pyropoikilocytosis

\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary pyropoikilocytosis
\Red blood cell disorder\Erythrocyte membrane abnormality\Hereditary pyropoikilocytosis

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary pyropoikilocytosis
\Disease\Disorder of cellular component of blood\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary pyropoikilocytosis
\Disease\Disorder of cellular component of blood\Anemia\Anemia due to intrinsic red cell abnormality\Hereditary pyropoikilocytosis
\Disease\Disorder of cellular component of blood\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary pyropoikilocytosis
\Disease\Disorder of cellular component of blood\Red blood cell disorder\Erythrocyte membrane abnormality\Hereditary pyropoikilocytosis
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary pyropoikilocytosis
\Disease\Disorder of body system\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary pyropoikilocytosis
\Disease\Disorder of body system\Red blood cell disorder\Erythrocyte membrane abnormality\Hereditary pyropoikilocytosis

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

16531015 Hereditary pyropoikilocytosis en Synonym Active Entire term case insensitive SNOMED CT core module

16532010 HPP en Synonym Active Entire term case sensitive SNOMED CT core module

838264013 Hereditary pyropoikilocytosis (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

1235831017 HPP - Hereditary pyropoikilocytosis en Synonym Active Entire term case sensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Hereditary pyropoikilocytosis	Is a	Anemia due to intrinsic red cell abnormality	true	Inferred relationship	Existential restriction modifier
Hereditary pyropoikilocytosis	Is a	Erythrocyte membrane abnormality	true	Inferred relationship	Existential restriction modifier
Hereditary pyropoikilocytosis	Finding site	Erythrocyte	true	Inferred relationship	Existential restriction modifier	3
Hereditary pyropoikilocytosis	Finding site	Hematopoietic system structure	false	Inferred relationship	Existential restriction modifier
Hereditary pyropoikilocytosis	Has definitional manifestation	Erythropenia	false	Inferred relationship	Existential restriction modifier
Hereditary pyropoikilocytosis	Finding site	Hematopoietic system structure	false	Inferred relationship	Existential restriction modifier
Hereditary pyropoikilocytosis	Is a	Hereditary red blood cell disorder	true	Inferred relationship	Existential restriction modifier
Hereditary pyropoikilocytosis	Finding site	Body system structure	false	Inferred relationship	Existential restriction modifier
Hereditary pyropoikilocytosis	Has interpretation	Below reference range	false	Inferred relationship	Existential restriction modifier	1
Hereditary pyropoikilocytosis	Interprets	Measurement of total hemoglobin concentration	false	Inferred relationship	Existential restriction modifier	1
Hereditary pyropoikilocytosis	Has interpretation	Below reference range	false	Inferred relationship	Existential restriction modifier	2
Hereditary pyropoikilocytosis	Interprets	Red blood cell count	false	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
16531015	Hereditary pyropoikilocytosis	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
16532010	HPP	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
838264013	Hereditary pyropoikilocytosis (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module
1235831017	HPP - Hereditary pyropoikilocytosis	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module