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403253001: Hypermelanosis due to Cushing syndrome (disorder)


Status: current, Defined. Date: 31-Jan 2020. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
1771179019 Hypermelanosis due to Cushing syndrome (disorder) en Fully specified name Active Initial character case insensitive SNOMED CT core
1782317014 Hypermelanosis due to Cushing syndrome en Synonym Active Initial character case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hypermelanosis due to Cushing syndrome Is a Hypermelanosis due to endocrine disorder true Inferred relationship Some
Hypermelanosis due to Cushing syndrome Associated morphology Hyperpigmentation false Inferred relationship Some 1
Hypermelanosis due to Cushing syndrome Associated etiologic finding Cushing's syndrome false Inferred relationship Some
Hypermelanosis due to Cushing syndrome Finding site Structure of skin region false Inferred relationship Some 1
Hypermelanosis due to Cushing syndrome Due to Cushing's syndrome true Inferred relationship Some 2
Hypermelanosis due to Cushing syndrome Associated morphology Melanosis false Inferred relationship Some
Hypermelanosis due to Cushing syndrome Finding site Skin structure true Inferred relationship Some 1
Hypermelanosis due to Cushing syndrome Associated morphology Melanosis true Inferred relationship Some 1
Hypermelanosis due to Cushing syndrome 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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