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403261006: Skin pigmentation due to hemosiderosis (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2003. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
1771187018 Skin pigmentation due to hemosiderosis (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
1773704013 Skin pigmentation due to haemosiderosis en Synonym Active Entire term case insensitive SNOMED CT core module
1774990012 Skin pigmentation due to hemosiderosis en Synonym Active Entire term case insensitive SNOMED CT core module
1783785018 Cutaneous haemosiderosis en Synonym Active Entire term case insensitive SNOMED CT core module
1784171012 Cutaneous hemosiderosis en Synonym Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Skin pigmentation due to hemosiderosis Is a Endogenous non-melanin pigmentation true Inferred relationship Existential restriction modifier
Skin pigmentation due to hemosiderosis Finding site Skin structure true Inferred relationship Existential restriction modifier 2
Skin pigmentation due to hemosiderosis Due to Hemosiderosis true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Hemosiderin pigmentation of skin due to venous insufficiency Is a False Skin pigmentation due to hemosiderosis Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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