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254048001: Spondylodysplasia, Luton type (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
378188016 Spondylodysplasia, Luton type en Synonym Active Initial character case insensitive SNOMED CT core
644886010 Spondylodysplasia, Luton type (disorder) en Fully specified name Active Initial character case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Spondylodysplasia, Luton type Pathological process Pathological developmental process true Inferred relationship Some 1
Spondylodysplasia, Luton type Occurrence Congenital true Inferred relationship Some 1
Spondylodysplasia, Luton type Associated morphology Congenital dysplasia false Inferred relationship Some 1
Spondylodysplasia, Luton type Finding site Bone structure false Inferred relationship Some 1
Spondylodysplasia, Luton type Associated morphology Congenital dysplasia false Inferred relationship Some 1
Spondylodysplasia, Luton type Associated morphology Dysplasia true Inferred relationship Some 1
Spondylodysplasia, Luton type Finding site Skeletal system structure false Inferred relationship Some 1
Spondylodysplasia, Luton type Occurrence Congenital false Inferred relationship Some 2
Spondylodysplasia, Luton type Finding site Bone structure false Inferred relationship Some 2
Spondylodysplasia, Luton type Associated morphology Congenital dysplasia false Inferred relationship Some 2
Spondylodysplasia, Luton type Occurrence Congenital false Inferred relationship Some
Spondylodysplasia, Luton type Finding site Bone structure true Inferred relationship Some 1
Spondylodysplasia, Luton type Is a Spondylodysplastic group true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Musculoskeletal finding reference set

Problem/Diagnosis reference set

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