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403260007: Hypermelanosis of undetermined etiology (disorder)


Status: current, Primitive. Date: 31-Jul 2003. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
1771186010 Hypermelanosis of undetermined etiology (disorder) en Fully specified name Active Case insensitive SNOMED CT core
1773703019 Hypermelanosis of undetermined aetiology en Synonym Active Case insensitive SNOMED CT core
1774989015 Hypermelanosis of undetermined etiology en Synonym Active Case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


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

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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