254048001: Spondylodysplasia, Luton type (disorder)

SNOMED CT Concept\Clinical finding (finding)\...

\Musculoskeletal finding (finding)\Bone finding\Disorder of bone (disorder)\Disorder of bone development\Congenital anomaly of skeletal bone\Spondylodysplastic group (disorder)\Spondylodysplasia, Luton type
\Musculoskeletal finding (finding)\Disorder of musculoskeletal system (disorder)\Disorder of skeletal system\Skeletal dysplasia\Spondylodysplastic group (disorder)\Spondylodysplasia, Luton type
\Musculoskeletal finding (finding)\Disorder of musculoskeletal system (disorder)\Disorder of skeletal system\Disorder of bone (disorder)\Disorder of bone development\Congenital anomaly of skeletal bone\Spondylodysplastic group (disorder)\Spondylodysplasia, Luton type
\Musculoskeletal finding (finding)\Disorder of musculoskeletal system (disorder)\Congenital anomaly of musculoskeletal system\Skeletal dysplasia\Spondylodysplastic group (disorder)\Spondylodysplasia, Luton type
\Musculoskeletal finding (finding)\Disorder of musculoskeletal system (disorder)\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Spondylodysplastic group (disorder)\Spondylodysplasia, Luton type

\Disease\Disorder of foetus and/or newborn\Congenital disease\Congenital malformation\Congenital anomaly of musculoskeletal system\Skeletal dysplasia\Spondylodysplastic group (disorder)\Spondylodysplasia, Luton type
\Disease\Disorder of foetus and/or newborn\Congenital disease\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Spondylodysplastic group (disorder)\Spondylodysplasia, Luton type
\Disease\Disorder of body system\Disorder of musculoskeletal system (disorder)\Disorder of skeletal system\Skeletal dysplasia\Spondylodysplastic group (disorder)\Spondylodysplasia, Luton type
\Disease\Disorder of body system\Disorder of musculoskeletal system (disorder)\Disorder of skeletal system\Disorder of bone (disorder)\Disorder of bone development\Congenital anomaly of skeletal bone\Spondylodysplastic group (disorder)\Spondylodysplasia, Luton type
\Disease\Disorder of body system\Disorder of musculoskeletal system (disorder)\Congenital anomaly of musculoskeletal system\Skeletal dysplasia\Spondylodysplastic group (disorder)\Spondylodysplasia, Luton type
\Disease\Disorder of body system\Disorder of musculoskeletal system (disorder)\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Spondylodysplastic group (disorder)\Spondylodysplasia, Luton type
\Disease\Developmental disorder (disorder)\Disorder of bone development\Congenital anomaly of skeletal bone\Spondylodysplastic group (disorder)\Spondylodysplasia, Luton type
\Disease\Developmental disorder (disorder)\Congenital malformation\Congenital anomaly of musculoskeletal system\Skeletal dysplasia\Spondylodysplastic group (disorder)\Spondylodysplasia, Luton type
\Disease\Developmental disorder (disorder)\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Spondylodysplastic group (disorder)\Spondylodysplasia, Luton type

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

378188016 Spondylodysplasia, Luton type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

644886010 Spondylodysplasia, Luton type (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

378188016 Spondylodysplasia, Luton type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

644886010 Spondylodysplasia, Luton type (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

5081501000241115 spondylodysplasie de type Luton fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

5081501000241115 spondylodysplasie de type Luton fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Spondylodysplasia, Luton type	Is a	Spondylodysplastic group (disorder)	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Spondylodysplasia, Luton type	Associated morphology	Dysplasia	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Spondylodysplasia, Luton type	Finding site	Skeletal system structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Spondylodysplasia, Luton type	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Spondylodysplasia, Luton type	Finding site	Bone structure	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Spondylodysplasia, Luton type	Associated morphology	Congenital dysplasia	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Spondylodysplasia, Luton type	Finding site	Bone structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Spondylodysplasia, Luton type	Associated morphology	Congenital dysplasia	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Spondylodysplasia, Luton type	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Spondylodysplasia, Luton type	Finding site	Bone structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Spondylodysplasia, Luton type	Associated morphology	Congenital dysplasia	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Spondylodysplasia, Luton type	Pathological process (attribute)	Pathological developmental process (qualifier value)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Spondylodysplasia, Luton type	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
378188016	Spondylodysplasia, Luton type	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
644886010	Spondylodysplasia, Luton type (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
378188016	Spondylodysplasia, Luton type	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
644886010	Spondylodysplasia, Luton type (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
5081501000241115	spondylodysplasie de type Luton	fr	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
5081501000241115	spondylodysplasie de type Luton	fr	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module