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238700008: Universal acquired melanosis (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
357760018 Universal acquired melanosis en Synonym Active Case insensitive SNOMED CT core
627616019 Universal acquired melanosis (disorder) en Fully specified name Active Case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


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