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403260007: Hypermelanosis of undetermined etiology (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
1771186010 Hypermelanosis of undetermined etiology (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
1773703019 Hypermelanosis of undetermined aetiology en Synonym Active Entire term case insensitive SNOMED CT core module
1774989015 Hypermelanosis of undetermined etiology 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
Hypermelanosis of undetermined etiology Is a Acquired hypermelanotic disorder true Inferred relationship Existential restriction modifier
Hypermelanosis of undetermined etiology Finding site Structure of skin region false Inferred relationship Existential restriction modifier 1
Hypermelanosis of undetermined etiology Associated morphology Hyperpigmentation false Inferred relationship Existential restriction modifier 1
Hypermelanosis of undetermined etiology Associated morphology Melanosis false Inferred relationship Existential restriction modifier
Hypermelanosis of undetermined etiology Occurrence Period of life beginning after birth and ending before death true Inferred relationship Existential restriction modifier 1
Hypermelanosis of undetermined etiology Finding site Skin structure true Inferred relationship Existential restriction modifier 1
Hypermelanosis of undetermined etiology Associated morphology Melanosis true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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