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398900000: Lentigo simplex (disorder)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 01-Nov 2023. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
1766820019 Lentigo simplex (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1778384014 Lentigo simplex en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5282636018 Simple lentigo en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1766820019 Lentigo simplex (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1766820019 Lentigo simplex (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1778384014 Lentigo simplex en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1778384014 Lentigo simplex en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5282636018 Simple lentigo en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5255981000241116 lentigo simplex fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5255981000241116 lentigo simplex fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Lentigo simplex (disorder) Is a Hyperpigmentation of skin false Inferred relationship Existential restriction modifier (core metadata concept)
Lentigo simplex (disorder) Associated morphology Hyperpigmentation (morphologic abnormality) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Lentigo simplex (disorder) Finding site Structure of skin region (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Lentigo simplex (disorder) Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Lentigo simplex (disorder) Is a lentigo false Inferred relationship Existential restriction modifier (core metadata concept)
Lentigo simplex (disorder) Associated morphology Increased melanin pigmentation false Inferred relationship Existential restriction modifier (core metadata concept) 1
Lentigo simplex (disorder) Associated morphology Increased melanin pigmentation false Inferred relationship Existential restriction modifier (core metadata concept) 1
Lentigo simplex (disorder) Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Lentigo simplex (disorder) Finding site Structure of skin and/or mucous membrane (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Lentigo simplex (disorder) Associated morphology Lentigo false Inferred relationship Existential restriction modifier (core metadata concept) 1
Lentigo simplex (disorder) Is a Lentiginosis true Inferred relationship Existential restriction modifier (core metadata concept)
Lentigo simplex (disorder) Is a Melanocytic nevus (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Lentigo simplex (disorder) Associated morphology Simple lentigo true Inferred relationship Existential restriction modifier (core metadata concept) 1
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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