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9434008: Hereditary pyropoikilocytosis (disorder)


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


0 descendants.

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

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