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403253001: Hypermelanosis due to Cushing syndrome (disorder)


Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jan 2020. Module: SNOMED CT core module

Descriptions:

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


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 Existential restriction modifier
Hypermelanosis due to Cushing syndrome Associated morphology Hyperpigmentation false Inferred relationship Existential restriction modifier 1
Hypermelanosis due to Cushing syndrome Associated etiologic finding Hypercortisolism false Inferred relationship Existential restriction modifier
Hypermelanosis due to Cushing syndrome Finding site Structure of skin region false Inferred relationship Existential restriction modifier 1
Hypermelanosis due to Cushing syndrome Due to Hypercortisolism true Inferred relationship Existential restriction modifier 2
Hypermelanosis due to Cushing syndrome Associated morphology Melanosis false Inferred relationship Existential restriction modifier
Hypermelanosis due to Cushing syndrome Finding site Skin structure true Inferred relationship Existential restriction modifier 1
Hypermelanosis due to Cushing syndrome Associated morphology Melanosis true Inferred relationship Existential restriction modifier 1
Hypermelanosis due to Cushing syndrome Occurrence Period of life beginning after birth and ending before death true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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