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39011001: Hemosiderosis (disorder)

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

Descriptions:

Id Description Lang Type Status Case? Module
491882015 Haemosiderosis en Synonym Active Case insensitive SNOMED CT core
65441014 Hemosiderosis en Synonym Active Case insensitive SNOMED CT core
775386018 Hemosiderosis (disorder) en Fully specified name Active Case insensitive SNOMED CT core

10 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Haemosiderosis Is a Iron overload true Inferred relationship Some
Haemosiderosis Causative agent Iron AND/OR iron compound false Inferred relationship Some
Haemosiderosis Causative agent Iron false Inferred relationship Some
Haemosiderosis Finding site Body system structure false Inferred relationship Some
Haemosiderosis Causative agent Iron and/or iron compound true Inferred relationship Some 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Haemosiderosis, acquired Is a True Haemosiderosis Inferred relationship Some
Secondary haemosiderosis Is a True Haemosiderosis Inferred relationship Some
Idiopathic pulmonary haemosiderosis Is a True Haemosiderosis Inferred relationship Some
Focal haemosiderosis Is a True Haemosiderosis Inferred relationship Some
Transfusion haemosiderosis Is a True Haemosiderosis Inferred relationship Some
Renal haemosiderosis Is a True Haemosiderosis Inferred relationship Some
Hepatic haemosiderosis Is a True Haemosiderosis Inferred relationship Some
Skin pigmentation due to haemosiderosis Due to True Haemosiderosis Inferred relationship Some 1

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Australian dialect reference set

Problem/Diagnosis reference set

Strength reference set

Description inactivation indicator reference set

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