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890235002: Autosomal recessive epidermolytic ichthyosis (disorder)


Status: current, Primitive. Date: 31-Jan 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
4011667017 Autosomal recessive epidermolytic ichthyosis (disorder) en Fully specified name Active Case insensitive SNOMED CT core
4011668010 Autosomal recessive epidermolytic ichthyosis en Synonym Active Case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Autosomal recessive epidermolytic ichthyosis Is a Autosomal recessive ichthyosis true Inferred relationship Some
Autosomal recessive epidermolytic ichthyosis Is a Keratinopathic ichthyosis true Inferred relationship Some
Autosomal recessive epidermolytic ichthyosis Finding site Entire skin true Inferred relationship Some 1
Autosomal recessive epidermolytic ichthyosis Occurrence Congenital true Inferred relationship Some 1
Autosomal recessive epidermolytic ichthyosis Pathological process Pathological developmental process true Inferred relationship Some 1
Autosomal recessive epidermolytic ichthyosis Associated morphology Hyperkeratosis true Inferred relationship Some 1
Autosomal recessive epidermolytic ichthyosis Has interpretation Abnormal true Inferred relationship Some 2
Autosomal recessive epidermolytic ichthyosis Interprets Keratinisation true Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Clinical finding foundation reference set

Problem/Diagnosis reference set

Description inactivation indicator reference set

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