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67202007: Ehlers-Danlos syndrome, type 5 (disorder)


Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
111647010 Ehlers-Danlos syndrome, type 5 en Synonym Active Case sensitive SNOMED CT core
111648017 Ehlers-Danlos syndrome, mild x-linked en Synonym Active Case sensitive SNOMED CT core
3789636010 X-linked Ehlers-Danlos syndrome en Synonym Active Case sensitive SNOMED CT core
500658014 Ehlers-Danlos syndrome type V en Synonym Active Case sensitive SNOMED CT core
806901018 Ehlers-Danlos syndrome, type 5 (disorder) en Fully specified name Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Ehlers-Danlos syndrome, type 5 Pathological process Pathological developmental process true Inferred relationship Some 1
Ehlers-Danlos syndrome, type 5 Pathological process Pathological developmental process true Inferred relationship Some 2
Ehlers-Danlos syndrome, type 5 Pathological process Pathological developmental process true Inferred relationship Some 3
Ehlers-Danlos syndrome, type 5 Associated morphology Dysplasia true Inferred relationship Some 2
Ehlers-Danlos syndrome, type 5 Associated morphology Dysplasia true Inferred relationship Some 3
Ehlers-Danlos syndrome, type 5 Occurrence Congenital true Inferred relationship Some 1
Ehlers-Danlos syndrome, type 5 Associated morphology Morphologically abnormal structure true Inferred relationship Some 1
Ehlers-Danlos syndrome, type 5 Is a X-linked hereditary disease false Inferred relationship Some
Ehlers-Danlos syndrome, type 5 Is a X-linked recessive hereditary disease true Inferred relationship Some
Ehlers-Danlos syndrome, type 5 Associated morphology Congenital dysplasia false Inferred relationship Some 1
Ehlers-Danlos syndrome, type 5 Is a Ehlers-Danlos syndrome true Inferred relationship Some
Ehlers-Danlos syndrome, type 5 Is a Ehlers-Danlos syndrome false Inferred relationship Some
Ehlers-Danlos syndrome, type 5 Finding site Bone structure false Inferred relationship Some 1
Ehlers-Danlos syndrome, type 5 Finding site Skin structure false Inferred relationship Some 1
Ehlers-Danlos syndrome, type 5 Associated morphology Congenital dysplasia false Inferred relationship Some 1
Ehlers-Danlos syndrome, type 5 Occurrence Congenital true Inferred relationship Some 2
Ehlers-Danlos syndrome, type 5 Associated morphology Congenital dysplasia false Inferred relationship Some 2
Ehlers-Danlos syndrome, type 5 Finding site Bone structure false Inferred relationship Some 2
Ehlers-Danlos syndrome, type 5 Occurrence Congenital true Inferred relationship Some 3
Ehlers-Danlos syndrome, type 5 Associated morphology Congenital dysplasia false Inferred relationship Some 3
Ehlers-Danlos syndrome, type 5 Finding site Skin structure false Inferred relationship Some 3
Ehlers-Danlos syndrome, type 5 Finding site Skin structure true Inferred relationship Some 2
Ehlers-Danlos syndrome, type 5 Finding site Bone structure true Inferred relationship Some 3
Ehlers-Danlos syndrome, type 5 Finding site Connective tissue false Inferred relationship Some
Ehlers-Danlos syndrome, type 5 Finding site Skin structure false Inferred relationship Some 1
Ehlers-Danlos syndrome, type 5 Finding site Skeletal system structure false Inferred relationship Some 1
Ehlers-Danlos syndrome, type 5 Occurrence Congenital false Inferred relationship Some
Ehlers-Danlos syndrome, type 5 Finding site Bone structure false Inferred relationship Some 1
Ehlers-Danlos syndrome, type 5 Severity Mild false Inferred relationship Some
Ehlers-Danlos syndrome, type 5 Finding site Connective tissue structure true Inferred relationship Some 1
Ehlers-Danlos syndrome, type 5 Associated morphology Dysplasia false Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Australian dialect reference set

Musculoskeletal finding reference set

Problem/Diagnosis reference set

Description inactivation indicator reference set

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