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890235002: Autosomal recessive epidermolytic ichthyosis (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). 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 Entire term case insensitive (core metadata concept) SNOMED CT core
4011668010 Autosomal recessive epidermolytic ichthyosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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