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9434008: Hereditary pyropoikilocytosis (disorder)


Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
1235831017 HPP - Hereditary pyropoikilocytosis en Synonym Active Case sensitive SNOMED CT core
16531015 Hereditary pyropoikilocytosis en Synonym Active Case insensitive SNOMED CT core
16532010 HPP en Synonym Active Case sensitive SNOMED CT core
838264013 Hereditary pyropoikilocytosis (disorder) en Fully specified name Active Case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hereditary pyropoikilocytosis Has definitional manifestation Erythropenia false Inferred relationship Some
Hereditary pyropoikilocytosis Finding site Haematopoietic system structure false Inferred relationship Some
Hereditary pyropoikilocytosis Is a Hereditary red blood cell disorder true Inferred relationship Some
Hereditary pyropoikilocytosis Finding site Body system structure false Inferred relationship Some
Hereditary pyropoikilocytosis Is a Anaemia due to intrinsic red cell abnormality true Inferred relationship Some
Hereditary pyropoikilocytosis Is a Erythrocyte membrane abnormality true Inferred relationship Some
Hereditary pyropoikilocytosis Has interpretation Below reference range false Inferred relationship Some 1
Hereditary pyropoikilocytosis Interprets Measurement of total haemoglobin concentration false Inferred relationship Some 1
Hereditary pyropoikilocytosis Has interpretation Below reference range false Inferred relationship Some 2
Hereditary pyropoikilocytosis Interprets Red blood cell count false Inferred relationship Some 2
Hereditary pyropoikilocytosis Finding site Erythrocyte true Inferred relationship Some 3
Hereditary pyropoikilocytosis Finding site Haematopoietic system structure false Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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