5731000119108: Congenital osteodystrophy (disorder)

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

\Musculoskeletal finding (finding)\Bone finding\Disorder of bone (disorder)\Degenerative disorder of bone\Osteodystrophy\Congenital osteodystrophy
\Musculoskeletal finding (finding)\Disorder of musculoskeletal system (disorder)\Degenerative disorder of musculoskeletal system (disorder)\Degenerative disorder of bone\Osteodystrophy\Congenital osteodystrophy
\Musculoskeletal finding (finding)\Disorder of musculoskeletal system (disorder)\Disorder of skeletal system\Disorder of bone (disorder)\Degenerative disorder of bone\Osteodystrophy\Congenital osteodystrophy

\Disease\Disorder of foetus and/or newborn\Congenital disease\Congenital osteodystrophy
\Disease\Degenerative disorder\Degenerative disorder of musculoskeletal system (disorder)\Degenerative disorder of bone\Osteodystrophy\Congenital osteodystrophy
\Disease\Disorder of body system\Disorder of musculoskeletal system (disorder)\Degenerative disorder of musculoskeletal system (disorder)\Degenerative disorder of bone\Osteodystrophy\Congenital osteodystrophy
\Disease\Disorder of body system\Disorder of musculoskeletal system (disorder)\Disorder of skeletal system\Disorder of bone (disorder)\Degenerative disorder of bone\Osteodystrophy\Congenital osteodystrophy

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2014. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

3004456012 Congenital osteodystrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

45771000119115 Congenital osteodystrophy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

3004456012 Congenital osteodystrophy en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

3004456012 Congenital osteodystrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

45771000119115 Congenital osteodystrophy (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

45771000119115 Congenital osteodystrophy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

5858971000241117 ostéodystrophie congénitale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

5858971000241117 ostéodystrophie congénitale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Congenital osteodystrophy	Is a	Disorder of bone (disorder)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital osteodystrophy	Is a	Degenerative disorder	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital osteodystrophy	Is a	Congenital connective tissue disorder	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital osteodystrophy	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital osteodystrophy	Associated morphology	Dystrophy	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital osteodystrophy	Finding site	Bone structure	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital osteodystrophy	Is a	Congenital disease	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital osteodystrophy	Is a	Osteodystrophy	true	Inferred relationship	Existential restriction modifier (core metadata concept)

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
DOORS syndrome	Is a	True	Congenital osteodystrophy	Inferred relationship	Existential restriction modifier (core metadata concept)
Francois syndrome	Is a	True	Congenital osteodystrophy	Inferred relationship	Existential restriction modifier (core metadata concept)
Morquio syndrome (disorder)	Is a	True	Congenital osteodystrophy	Inferred relationship	Existential restriction modifier (core metadata concept)

This concept is not in any reference sets