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1255143006: Ichthyosis hystrix gravior (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
5144603018 Ichthyosis hystrix gravior (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
5144604012 Ichthyosis Lambert type en Synonym Active Only initial character case insensitive SNOMED CT core module
5144605013 Ichthyosis hystrix gravior en Synonym Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Ichthyosis hystrix gravior Is a Autosomal dominant ichthyosis true Inferred relationship Existential restriction modifier
Ichthyosis hystrix gravior Is a Ichthyosis hystrix true Inferred relationship Existential restriction modifier
Ichthyosis hystrix gravior Interprets Keratinization, function true Inferred relationship Existential restriction modifier 2
Ichthyosis hystrix gravior Has interpretation Abnormal true Inferred relationship Existential restriction modifier 2
Ichthyosis hystrix gravior Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Ichthyosis hystrix gravior Finding site Entire skin true Inferred relationship Existential restriction modifier 1
Ichthyosis hystrix gravior Associated morphology Hyperkeratosis true Inferred relationship Existential restriction modifier 1
Ichthyosis hystrix gravior Pathological process Pathological developmental process 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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