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398900000: Lentigo simplex (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
1766820019 Lentigo simplex (disorder) en Fully specified name Active Case insensitive SNOMED CT core
1778384014 Lentigo simplex en Synonym Active Case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Lentigo simplex Is a Hyperpigmentation of skin false Inferred relationship Some
Lentigo simplex Associated morphology Hyperpigmentation false Inferred relationship Some 1
Lentigo simplex Finding site Structure of skin region false Inferred relationship Some 1
Lentigo simplex Finding site Skin structure false Inferred relationship Some 1
Lentigo simplex Is a Lentigo false Inferred relationship Some
Lentigo simplex Associated morphology Increased melanin pigmentation false Inferred relationship Some 1
Lentigo simplex Associated morphology Increased melanin pigmentation false Inferred relationship Some 1
Lentigo simplex Finding site Skin structure false Inferred relationship Some 1
Lentigo simplex Finding site Structure of skin and/or mucous membrane true Inferred relationship Some 1
Lentigo simplex Associated morphology Lentigo true Inferred relationship Some 1
Lentigo simplex Is a Lentiginosis true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Neoplasm and/or hamartoma reference set

Problem/Diagnosis reference set

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