401138005: sequentie van foetale akinesie en deformatie (aandoening)

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

\Deformity (finding)\Congenital deformity\Arthrogryposis\Arthrogryposis multiplex congenita\Pena-Shokeir syndrome type I (disorder)
\Deformity (finding)\Congenital deformity\Arthrogryposis\Inherited arthrogryposis\Pena-Shokeir syndrome type I (disorder)
\Deformity (finding)\Contracture of joint\Contracture of multiple joints\Arthrogryposis\Arthrogryposis multiplex congenita\Pena-Shokeir syndrome type I (disorder)
\Deformity (finding)\Contracture of joint\Contracture of multiple joints\Arthrogryposis\Inherited arthrogryposis\Pena-Shokeir syndrome type I (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\Arthrogryposis multiplex congenita\Pena-Shokeir syndrome type I (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\Inherited arthrogryposis\Pena-Shokeir syndrome type I (disorder)
\Finding of movement (finding)\Movement disorder\Contracture of joint\Contracture of multiple joints\Arthrogryposis\Arthrogryposis multiplex congenita\Pena-Shokeir syndrome type I (disorder)
\Finding of movement (finding)\Movement disorder\Contracture of joint\Contracture of multiple joints\Arthrogryposis\Inherited arthrogryposis\Pena-Shokeir syndrome type I (disorder)

\Disease\Disorder of joint region\Contracture of joint\Contracture of multiple joints\Arthrogryposis\Arthrogryposis multiplex congenita\Pena-Shokeir syndrome type I (disorder)
\Disease\Disorder of joint region\Contracture of joint\Contracture of multiple joints\Arthrogryposis\Inherited arthrogryposis\Pena-Shokeir syndrome type I (disorder)
\Disease\Genetic disease\Hereditary disease\Developmental hereditary disorder\Inherited arthrogryposis\Pena-Shokeir syndrome type I (disorder)
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Pena-Shokeir syndrome type I (disorder)
\Disease\Disorder of foetus and/or newborn\Congenital disease (disorder)\Congenital malformation\Congenital malformation syndrome (disorder)\Multiple system malformation syndrome\Multiple malformation syndrome with unusual brain and/or neuromuscular findings\Pena-Shokeir syndrome type I (disorder)
\Disease\Disorder of foetus and/or newborn\Congenital disease (disorder)\Congenital malformation\Congenital deformity\Arthrogryposis\Arthrogryposis multiplex congenita\Pena-Shokeir syndrome type I (disorder)
\Disease\Disorder of foetus and/or newborn\Congenital disease (disorder)\Congenital malformation\Congenital deformity\Arthrogryposis\Inherited arthrogryposis\Pena-Shokeir syndrome type I (disorder)
\Disease\Movement disorder\Contracture of joint\Contracture of multiple joints\Arthrogryposis\Arthrogryposis multiplex congenita\Pena-Shokeir syndrome type I (disorder)
\Disease\Movement disorder\Contracture of joint\Contracture of multiple joints\Arthrogryposis\Inherited arthrogryposis\Pena-Shokeir syndrome type I (disorder)
\Disease\Developmental disorder\Developmental hereditary disorder\Inherited arthrogryposis\Pena-Shokeir syndrome type I (disorder)
\Disease\Developmental disorder\Congenital malformation\Congenital malformation syndrome (disorder)\Multiple system malformation syndrome\Multiple malformation syndrome with unusual brain and/or neuromuscular findings\Pena-Shokeir syndrome type I (disorder)
\Disease\Developmental disorder\Congenital malformation\Congenital deformity\Arthrogryposis\Arthrogryposis multiplex congenita\Pena-Shokeir syndrome type I (disorder)
\Disease\Developmental disorder\Congenital malformation\Congenital deformity\Arthrogryposis\Inherited arthrogryposis\Pena-Shokeir syndrome type I (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2003. Module: SNOMED CT core

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Pena-Shokeir syndrome type I (disorder)	Is a	Pena-Shokeir-fenotype	false	Inferred relationship	Some
Pena-Shokeir syndrome type I (disorder)	Finding site	Brain structure	false	Inferred relationship	Some	1
Pena-Shokeir syndrome type I (disorder)	Associated morphology	Congenital malformation	false	Inferred relationship	Some
Pena-Shokeir syndrome type I (disorder)	Occurrence	Congenital	false	Inferred relationship	Some
Pena-Shokeir syndrome type I (disorder)	Occurrence	Congenital	true	Inferred relationship	Some	1
Pena-Shokeir syndrome type I (disorder)	Associated morphology	gebrekkige ontwikkeling (afwijkende morfologie)	false	Inferred relationship	Some	1
Pena-Shokeir syndrome type I (disorder)	Associated morphology	Morphologically abnormal structure (morphologic abnormality)	false	Inferred relationship	Some	1
Pena-Shokeir syndrome type I (disorder)	Pathological process (attribute)	Pathological developmental process	true	Inferred relationship	Some	1
Pena-Shokeir syndrome type I (disorder)	Is a	Multiple malformation syndrome with unusual brain and/or neuromuscular findings	true	Inferred relationship	Some
Pena-Shokeir syndrome type I (disorder)	Is a	Arthrogryposis multiplex congenita	true	Inferred relationship	Some
Pena-Shokeir syndrome type I (disorder)	Is a	Inherited arthrogryposis	true	Inferred relationship	Some
Pena-Shokeir syndrome type I (disorder)	Is a	Autosomal recessive hereditary disorder	true	Inferred relationship	Some
Pena-Shokeir syndrome type I (disorder)	Interprets	Range of joint movement	true	Inferred relationship	Some	2
Pena-Shokeir syndrome type I (disorder)	Has interpretation	Decreased	true	Inferred relationship	Some	2
Pena-Shokeir syndrome type I (disorder)	Finding site	Structure of joint region	true	Inferred relationship	Some	1
Pena-Shokeir syndrome type I (disorder)	Associated morphology	Contracture	true	Inferred relationship	Some	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

Dutch pathology simple reference set (foundation metadata concept)

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Id	Description	Lang	Type	Status	Case?	Module
1769059014	Pena-Shokeir syndrome type I (disorder)	en	Fully specified name	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
1780339018	Pena-Shokeir syndrome type I	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
1787452014	Fetal akinesia-hypokinesia sequence	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
1787454010	Foetal akinesia-hypokinesia sequence	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
5171547012	Arthrogryposis multiplex congenita, pulmonary hypoplasia syndrome	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
5171548019	FADS - foetal akinesia deformation sequence	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
5171549010	FADS - fetal akinesia deformation sequence	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
6707981000146114	syndroom van Pena-Shokeir type 1	nl	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
6707991000146111	FADS	nl	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
6708001000146115	foetale akinesiesequentie	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
6708031000146113	Pena-Shokeir-syndroom type 1	nl	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
8526231000146119	sequentie van foetale akinesie en deformatie (aandoening)	nl	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
8526241000146110	sequentie van foetale akinesie en deformatie	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
8526251000146113	sequentie van foetale akinesie en hypokinesie	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
8526261000146111	foetale akinesiehypokinesiesequentie	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
8721091000146119	foetale akinesiedeformatiesequentie	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)