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398900000: Lentigo simplex (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
1766820019 Lentigo simplex (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
1778384014 Lentigo simplex 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
Lentigo simplex Is a Hyperpigmentation of skin false Inferred relationship Existential restriction modifier
Lentigo simplex Associated morphology Hyperpigmentation false Inferred relationship Existential restriction modifier 1
Lentigo simplex Finding site Structure of skin region false Inferred relationship Existential restriction modifier 1
Lentigo simplex Finding site Skin structure false Inferred relationship Existential restriction modifier 1
Lentigo simplex Is a Lentigo false Inferred relationship Existential restriction modifier
Lentigo simplex Associated morphology Increased melanin pigmentation false Inferred relationship Existential restriction modifier 1
Lentigo simplex Associated morphology Increased melanin pigmentation false Inferred relationship Existential restriction modifier 1
Lentigo simplex Finding site Skin structure false Inferred relationship Existential restriction modifier 1
Lentigo simplex Finding site Structure of skin and/or mucous membrane true Inferred relationship Existential restriction modifier 1
Lentigo simplex Associated morphology Lentigo true Inferred relationship Existential restriction modifier 1
Lentigo simplex Is a Lentiginosis true Inferred relationship Existential restriction modifier
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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