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715318006: Ehlers-Danlos syndrome classic type (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
3302210017 Ehlers-Danlos syndrome classic type (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module
3302211018 Ehlers-Danlos syndrome classic type en Synonym Active Entire term case sensitive SNOMED CT core module
3302212013 Ehlers-Danlos syndrome classical type en Synonym Active Entire term case sensitive SNOMED CT core module


2 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Ehlers-Danlos syndrome classic type Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Ehlers-Danlos syndrome classic type Is a Ehlers-Danlos syndrome true Inferred relationship Existential restriction modifier
Ehlers-Danlos syndrome classic type Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier 2
Ehlers-Danlos syndrome classic type Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Ehlers-Danlos syndrome classic type Finding site Bone structure true Inferred relationship Existential restriction modifier 2
Ehlers-Danlos syndrome classic type Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier 3
Ehlers-Danlos syndrome classic type Occurrence Congenital true Inferred relationship Existential restriction modifier 3
Ehlers-Danlos syndrome classic type Finding site Skin structure false Inferred relationship Existential restriction modifier 2
Ehlers-Danlos syndrome classic type Finding site Bone structure false Inferred relationship Existential restriction modifier 3
Ehlers-Danlos syndrome classic type Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Ehlers-Danlos syndrome classic type Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Ehlers-Danlos syndrome classic type Finding site Skin structure true Inferred relationship Existential restriction modifier 1
Ehlers-Danlos syndrome classic type Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Ehlers-Danlos syndrome classic type Is a Connective tissue hereditary disorder false Inferred relationship Existential restriction modifier
Ehlers-Danlos syndrome classic type Is a Hereditary disorder of the integument false Inferred relationship Existential restriction modifier
Ehlers-Danlos syndrome classic type Is a Hereditary disorder of musculoskeletal system false Inferred relationship Existential restriction modifier
Ehlers-Danlos syndrome classic type Associated morphology Dysplasia true Inferred relationship Existential restriction modifier 1
Ehlers-Danlos syndrome classic type Associated morphology Dysplasia true Inferred relationship Existential restriction modifier 2
Ehlers-Danlos syndrome classic type Finding site Connective tissue structure true Inferred relationship Existential restriction modifier 3
Ehlers-Danlos syndrome classic type Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 3
Ehlers-Danlos syndrome classic type Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 3

Inbound Relationships Type Active Source Characteristic Refinability Group
Ehlers-Danlos syndrome, type 2 Is a True Ehlers-Danlos syndrome classic type Inferred relationship Existential restriction modifier
Ehlers-Danlos syndrome, type 1 Is a True Ehlers-Danlos syndrome classic type Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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