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402621008: Idiopathic vitiligo (disorder)


Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jul 2021. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
1770545016 Idiopathic vitiligo (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
1781735017 Idiopathic vitiligo 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
Idiopathic vitiligo Is a Vitiligo true Inferred relationship Existential restriction modifier
Idiopathic vitiligo Associated morphology Structure showing abnormal deposition of pigment false Inferred relationship Existential restriction modifier 2
Idiopathic vitiligo Finding site Structure of skin region false Inferred relationship Existential restriction modifier 1
Idiopathic vitiligo Associated morphology Hypopigmentation false Inferred relationship Existential restriction modifier 1
Idiopathic vitiligo Finding site Skin structure false Inferred relationship Existential restriction modifier 1
Idiopathic vitiligo Finding site Skin structure false Inferred relationship Existential restriction modifier 2
Idiopathic vitiligo Associated morphology Hypopigmentation true Inferred relationship Existential restriction modifier 1
Idiopathic vitiligo Finding site Skin structure true Inferred relationship Existential restriction modifier 1
Idiopathic vitiligo Is a Idiopathic disease 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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