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239082002: Dyschromatosis universalis (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
358293012 Dyschromatosis universalis en Synonym Active Case insensitive SNOMED CT core
358294018 Melanism en Synonym Active Case insensitive SNOMED CT core
628050014 Dyschromatosis universalis (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
Dyschromatosis universalis Pathological process Pathological developmental process true Inferred relationship Some 1
Dyschromatosis universalis Associated morphology Hyperpigmentation true Inferred relationship Some 1
Dyschromatosis universalis Associated morphology Congenital anomaly false Inferred relationship Some 1
Dyschromatosis universalis Finding site Skin structure false Inferred relationship Some 2
Dyschromatosis universalis Finding site Skin structure false Inferred relationship Some 1
Dyschromatosis universalis Finding site Skin structure false Inferred relationship Some 2
Dyschromatosis universalis Finding site Skin structure false Inferred relationship Some 1
Dyschromatosis universalis Finding site Skin structure false Inferred relationship Some 2
Dyschromatosis universalis Finding site Skin structure false Inferred relationship Some 1
Dyschromatosis universalis Finding site Skin structure false Inferred relationship Some 2
Dyschromatosis universalis Finding site Skin structure false Inferred relationship Some 1
Dyschromatosis universalis Finding site Skin structure false Inferred relationship Some 2
Dyschromatosis universalis Associated morphology Hyperpigmentation false Inferred relationship Some 2
Dyschromatosis universalis Finding site Skin structure true Inferred relationship Some 1
Dyschromatosis universalis Occurrence Congenital false Inferred relationship Some 3
Dyschromatosis universalis Associated morphology Developmental abnormality false Inferred relationship Some 3
Dyschromatosis universalis Finding site Skin structure false Inferred relationship Some 3
Dyschromatosis universalis Finding site Structure of skin region false Inferred relationship Some 1
Dyschromatosis universalis Occurrence Congenital false Inferred relationship Some
Dyschromatosis universalis Is a Inherited cutaneous hyperpigmentation true Inferred relationship Some
Dyschromatosis universalis Occurrence Congenital 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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