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724838009: Hereditary skin peeling syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2017. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3449166014 Hereditary skin peeling syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3449167017 Hereditary skin peeling syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
4594936015 Peeling skin syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
4594937012 Familial continuous skin peeling syndrome en Synonym Active Entire term case insensitive SNOMED CT core module


4 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hereditary skin peeling syndrome Is a Skin peeling disorder true Inferred relationship Existential restriction modifier
Hereditary skin peeling syndrome Is a Inherited disorder of keratinization false Inferred relationship Existential restriction modifier
Hereditary skin peeling syndrome Has definitional manifestation Abnormal keratinization false Inferred relationship Existential restriction modifier
Hereditary skin peeling syndrome Associated morphology Exfoliative lesion true Inferred relationship Existential restriction modifier 4
Hereditary skin peeling syndrome Finding site Skin structure true Inferred relationship Existential restriction modifier 4
Hereditary skin peeling syndrome Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 5
Hereditary skin peeling syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 5
Hereditary skin peeling syndrome Finding site Skin structure false Inferred relationship Existential restriction modifier 5
Hereditary skin peeling syndrome Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 1
Hereditary skin peeling syndrome Finding site Skin structure false Inferred relationship Existential restriction modifier 1
Hereditary skin peeling syndrome Has interpretation Abnormal true Inferred relationship Existential restriction modifier 3
Hereditary skin peeling syndrome Interprets Keratinization, function true Inferred relationship Existential restriction modifier 3
Hereditary skin peeling syndrome Is a Developmental hereditary disorder false Inferred relationship Existential restriction modifier
Hereditary skin peeling syndrome Associated morphology Morphologically abnormal structure false Inferred relationship Existential restriction modifier 2
Hereditary skin peeling syndrome Finding site Skin structure false Inferred relationship Existential restriction modifier 2
Hereditary skin peeling syndrome Pathological process Pathological developmental process false Inferred relationship Existential restriction modifier 2
Hereditary skin peeling syndrome Is a Autosomal recessive ichthyosis true Inferred relationship Existential restriction modifier
Hereditary skin peeling syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Hereditary skin peeling syndrome Finding site Entire skin true Inferred relationship Existential restriction modifier 1
Hereditary skin peeling syndrome Associated morphology Hyperkeratosis true Inferred relationship Existential restriction modifier 1
Hereditary skin peeling syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Generalized peeling skin syndrome Is a True Hereditary skin peeling syndrome Inferred relationship Existential restriction modifier
Acral peeling skin syndrome Is a True Hereditary skin peeling syndrome Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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