715216008: distale artrogrypose type 2B (aandoening)

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

\Deformity (finding)\Congenital deformity\Arthrogryposis\Distal arthrogryposis syndrome\Distal arthrogryposis type 2B (disorder)
\Deformity (finding)\Contracture of joint\Contracture of multiple joints\Arthrogryposis\Distal arthrogryposis syndrome\Distal arthrogryposis type 2B (disorder)

\Finding of movement (finding)\Finding of joint movement\Finding of range of joint movement\Limitation of joint movement\Contracture of joint\Contracture of multiple joints\Arthrogryposis\Distal arthrogryposis syndrome\Distal arthrogryposis type 2B (disorder)
\Finding of movement (finding)\Movement disorder\Contracture of joint\Contracture of multiple joints\Arthrogryposis\Distal arthrogryposis syndrome\Distal arthrogryposis type 2B (disorder)

\Disease\Disorder of joint region\Contracture of joint\Contracture of multiple joints\Arthrogryposis\Distal arthrogryposis syndrome\Distal arthrogryposis type 2B (disorder)
\Disease\Disorder of foetus and/or newborn\Congenital disease (disorder)\Congenital malformation\Congenital deformity\Arthrogryposis\Distal arthrogryposis syndrome\Distal arthrogryposis type 2B (disorder)
\Disease\Movement disorder\Contracture of joint\Contracture of multiple joints\Arthrogryposis\Distal arthrogryposis syndrome\Distal arthrogryposis type 2B (disorder)
\Disease\Developmental disorder\Congenital malformation\Congenital deformity\Arthrogryposis\Distal arthrogryposis syndrome\Distal arthrogryposis type 2B (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Distal arthrogryposis type 2B (disorder)	Is a	Distal arthrogryposis syndrome	true	Inferred relationship	Some
Distal arthrogryposis type 2B (disorder)	Associated morphology	Contracture	true	Inferred relationship	Some	1
Distal arthrogryposis type 2B (disorder)	Occurrence	Congenital	true	Inferred relationship	Some	1
Distal arthrogryposis type 2B (disorder)	Finding site	Joint structure	false	Inferred relationship	Some	1
Distal arthrogryposis type 2B (disorder)	Has interpretation	Decreased	true	Inferred relationship	Some	2
Distal arthrogryposis type 2B (disorder)	Pathological process (attribute)	Pathological developmental process	true	Inferred relationship	Some	1
Distal arthrogryposis type 2B (disorder)	Finding site	Structure of joint region	true	Inferred relationship	Some	1
Distal arthrogryposis type 2B (disorder)	Interprets	Range of joint movement	true	Inferred relationship	Some	2

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
3301893013	Distal arthrogryposis type 2B (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
3301894019	Distal arthrogryposis type 2B	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
3301895018	Sheldon-Hall syndrome	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
3301896017	Freeman-Sheldon syndrome variant	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
6471991000146118	distale artrogrypose type 2B	nl	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
6472001000146115	distale artrogrypose type 2B (aandoening)	nl	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
6472011000146118	Sheldon-Hall-syndroom	nl	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
6472021000146111	syndroom van Sheldon-Hall	nl	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
6472031000146113	Freeman-Sheldon-syndroomvariant	nl	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
3301897014	Rare multiple congenital contracture syndrome characterized by contractures of distal joints of the limbs, triangular face, downslanting palpebral fissures, small mouth, and high arched palate.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
3301964014	Rare multiple congenital contracture syndrome characterised by contractures of distal joints of the limbs, triangular face, downslanting palpebral fissures, small mouth, and high arched palate.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core