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717041008: Syndromic recessive X-linked ichthyosis (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2016. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3308247010 Syndromic recessive X-linked ichthyosis (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module
3308248017 Syndromic recessive X-linked ichthyosis en Synonym Active Only initial character case insensitive SNOMED CT core module
3308249013 Syndromic X-linked ichthyosis 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
Syndromic recessive X-linked ichthyosis Associated morphology Hyperkeratosis false Inferred relationship Existential restriction modifier
Syndromic recessive X-linked ichthyosis Is a X-linked ichthyosis with steryl-sulfatase deficiency true Inferred relationship Existential restriction modifier
Syndromic recessive X-linked ichthyosis Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 2
Syndromic recessive X-linked ichthyosis Occurrence Congenital false Inferred relationship Existential restriction modifier 2
Syndromic recessive X-linked ichthyosis Finding site Skin structure false Inferred relationship Existential restriction modifier 2
Syndromic recessive X-linked ichthyosis Finding site Skin structure false Inferred relationship Existential restriction modifier 1
Syndromic recessive X-linked ichthyosis Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Syndromic recessive X-linked ichthyosis Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Syndromic recessive X-linked ichthyosis Associated morphology Hyperkeratosis true Inferred relationship Existential restriction modifier 1
Syndromic recessive X-linked ichthyosis Has interpretation Abnormal true Inferred relationship Existential restriction modifier 2
Syndromic recessive X-linked ichthyosis Interprets Keratinization, function true Inferred relationship Existential restriction modifier 2
Syndromic recessive X-linked ichthyosis Finding site Entire skin 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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