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1254911003: Hypermelanotic pigmentary mosaicism (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Oct 2022. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
5143840019 Hypermelanotic pigmentary mosaicism en Synonym Active Entire term case insensitive SNOMED CT core module
5143841015 Hypermelanotic pigmentary mosaicism (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hypermelanotic pigmentary mosaicism Is a Genetic mosaic true Inferred relationship Existential restriction modifier
Hypermelanotic pigmentary mosaicism Is a Hereditary hypermelanosis true Inferred relationship Existential restriction modifier
Hypermelanotic pigmentary mosaicism Interprets Genetic test true Inferred relationship Existential restriction modifier 2
Hypermelanotic pigmentary mosaicism Finding site Skin structure true Inferred relationship Existential restriction modifier 1
Hypermelanotic pigmentary mosaicism Associated morphology Melanosis 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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