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49238001: Melanoderma (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
786894018 Melanoderma (disorder) en Fully specified name Active Case insensitive SNOMED CT core
82025016 Melanoderma en Synonym Active Case insensitive SNOMED CT core


4 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Melanoderma Is a Acquired hypermelanotic disorder true Inferred relationship Some
Melanoderma Is a Disorder of skin pigmentation false Inferred relationship Some
Melanoderma Is a Site-specific disorder of skin false Inferred relationship Some
Melanoderma Associated morphology Melanosis false Inferred relationship Some
Melanoderma Finding site Skin structure false Inferred relationship Some 1
Melanoderma Associated morphology Hyperpigmentation false Inferred relationship Some 1
Melanoderma Finding site Skin structure true Inferred relationship Some 1
Melanoderma Finding site Structure of skin region false Inferred relationship Some 1
Melanoderma Associated morphology Hyperpigmentation false Inferred relationship Some 1
Melanoderma Finding site Skin structure false Inferred relationship Some 1
Melanoderma Associated morphology Melanosis true Inferred relationship Some 1
Melanoderma Occurrence Period of life between birth and death true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Addison melanoderma Is a True Melanoderma Inferred relationship Some
Senile melanoderma Is a True Melanoderma Inferred relationship Some
Parasitic melanoderma Is a True Melanoderma Inferred relationship Some
Melanoderma cachecticorum Is a True Melanoderma Inferred relationship Some
Pigmented peribuccal erythrosis of Brocq Is a False Melanoderma Inferred relationship Some

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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