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1717003: Idiopathic guttate hypomelanosis (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
3036349016 Guttate hypomelanosis en Synonym Active Case insensitive SNOMED CT core
3969010 Idiopathic guttate hypomelanosis en Synonym Active Case insensitive SNOMED CT core
744337017 Idiopathic guttate hypomelanosis (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
Idiopathic guttate hypomelanosis Is a Idiopathic disease false Inferred relationship Some
Idiopathic guttate hypomelanosis Is a Disorder of skin pigmentation false Inferred relationship Some
Idiopathic guttate hypomelanosis Finding site Skin structure false Inferred relationship Some 1
Idiopathic guttate hypomelanosis Is a Acquired hypomelanosis of uncertain aetiology true Inferred relationship Some
Idiopathic guttate hypomelanosis Associated morphology Hypopigmentation false Inferred relationship Some
Idiopathic guttate hypomelanosis Associated morphology Decreased melanin pigmentation false Inferred relationship Some 1
Idiopathic guttate hypomelanosis Associated morphology Decreased melanin pigmentation true Inferred relationship Some 1
Idiopathic guttate hypomelanosis Finding site Skin structure true Inferred relationship Some 1
Idiopathic guttate hypomelanosis Associated morphology Depigmentation false Inferred relationship Some 2
Idiopathic guttate hypomelanosis Associated morphology Pigment deposition false Inferred relationship Some 1
Idiopathic guttate hypomelanosis Finding site Structure of skin region false Inferred relationship Some
Idiopathic guttate hypomelanosis Occurrence Period of life between birth and death true 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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