71322004: Familial articular hypermobility syndrome (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\Familial articular hypermobility syndrome (disorder)
\Musculoskeletal finding (finding)\Joint finding\Arthropathy\Familial articular hypermobility syndrome (disorder)
\Musculoskeletal finding (finding)\Joint finding\Joint laxity\Familial articular hypermobility syndrome (disorder)
\Musculoskeletal finding (finding)\Disorder of musculoskeletal system (disorder)\Hereditary disorder of musculoskeletal system\Familial articular hypermobility syndrome (disorder)
\Musculoskeletal finding (finding)\Disorder of musculoskeletal system (disorder)\Musculoskeletal and connective tissue disorder (disorder)\Familial articular hypermobility syndrome (disorder)
\Musculoskeletal finding (finding)\Disorder of musculoskeletal system (disorder)\Disorder of skeletal system\Arthropathy\Familial articular hypermobility syndrome (disorder)
\Musculoskeletal finding (finding)\Disorder of musculoskeletal system (disorder)\Disorder of skeletal system\Skeletal dysplasia\Familial articular hypermobility syndrome (disorder)
\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\Familial articular hypermobility syndrome (disorder)
\Musculoskeletal finding (finding)\Disorder of musculoskeletal system (disorder)\Congenital anomaly of musculoskeletal system\Skeletal dysplasia\Familial articular hypermobility syndrome (disorder)
\Musculoskeletal finding (finding)\Disorder of musculoskeletal system (disorder)\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Familial articular hypermobility syndrome (disorder)

\Disease\Disorder of joint region\Arthropathy\Familial articular hypermobility syndrome (disorder)
\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system (disorder)\Hereditary disorder of musculoskeletal system\Familial articular hypermobility syndrome (disorder)
\Disease\Genetic disease\Hereditary disease\Developmental hereditary disorder\Familial articular hypermobility syndrome (disorder)
\Disease\Genetic disease\Hereditary disease\Connective tissue hereditary disorder\Familial articular hypermobility syndrome (disorder)
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Familial articular hypermobility syndrome (disorder)
\Disease\Disorder of foetus and/or newborn\Congenital disease\Congenital connective tissue disorder\Familial articular hypermobility syndrome (disorder)
\Disease\Disorder of foetus and/or newborn\Congenital disease\Congenital malformation\Congenital anomaly of musculoskeletal system\Skeletal dysplasia\Familial articular hypermobility syndrome (disorder)
\Disease\Disorder of foetus and/or newborn\Congenital disease\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Familial articular hypermobility syndrome (disorder)
\Disease\Disorder of body system\Hereditary disorder by system (disorder)\Hereditary disorder of musculoskeletal system\Familial articular hypermobility syndrome (disorder)
\Disease\Disorder of body system\Disorder of musculoskeletal system (disorder)\Hereditary disorder of musculoskeletal system\Familial articular hypermobility syndrome (disorder)
\Disease\Disorder of body system\Disorder of musculoskeletal system (disorder)\Musculoskeletal and connective tissue disorder (disorder)\Familial articular hypermobility syndrome (disorder)
\Disease\Disorder of body system\Disorder of musculoskeletal system (disorder)\Disorder of skeletal system\Arthropathy\Familial articular hypermobility syndrome (disorder)
\Disease\Disorder of body system\Disorder of musculoskeletal system (disorder)\Disorder of skeletal system\Skeletal dysplasia\Familial articular hypermobility syndrome (disorder)
\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\Familial articular hypermobility syndrome (disorder)
\Disease\Disorder of body system\Disorder of musculoskeletal system (disorder)\Congenital anomaly of musculoskeletal system\Skeletal dysplasia\Familial articular hypermobility syndrome (disorder)
\Disease\Disorder of body system\Disorder of musculoskeletal system (disorder)\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Familial articular hypermobility syndrome (disorder)
\Disease\Disorder of connective tissue\Connective tissue hereditary disorder\Familial articular hypermobility syndrome (disorder)
\Disease\Disorder of connective tissue\Congenital connective tissue disorder\Familial articular hypermobility syndrome (disorder)
\Disease\Disorder of connective tissue\Musculoskeletal and connective tissue disorder (disorder)\Familial articular hypermobility syndrome (disorder)
\Disease\Developmental disorder (disorder)\Disorder of bone development\Congenital anomaly of skeletal bone\Familial articular hypermobility syndrome (disorder)
\Disease\Developmental disorder (disorder)\Developmental hereditary disorder\Familial articular hypermobility syndrome (disorder)
\Disease\Developmental disorder (disorder)\Congenital malformation\Congenital anomaly of musculoskeletal system\Skeletal dysplasia\Familial articular hypermobility syndrome (disorder)
\Disease\Developmental disorder (disorder)\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Familial articular hypermobility syndrome (disorder)

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

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Familial articular hypermobility syndrome (disorder)	Is a	Ehlers-Danlos syndrome	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Familial articular hypermobility syndrome (disorder)	Associated morphology	Abnormally increased laxity	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Familial articular hypermobility syndrome (disorder)	Finding site	Connective tissue structure (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	4
Familial articular hypermobility syndrome (disorder)	Associated morphology	Dysplasia	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Familial articular hypermobility syndrome (disorder)	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Familial articular hypermobility syndrome (disorder)	Finding site	Connective tissue	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Familial articular hypermobility syndrome (disorder)	Finding site	Skeletal system structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Familial articular hypermobility syndrome (disorder)	Finding site	Articular system structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Familial articular hypermobility syndrome (disorder)	Finding site	Bone structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Familial articular hypermobility syndrome (disorder)	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Familial articular hypermobility syndrome (disorder)	Associated morphology	Congenital dysplasia	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Familial articular hypermobility syndrome (disorder)	Is a	Ehlers-Danlos syndrome (disorder)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Familial articular hypermobility syndrome (disorder)	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Familial articular hypermobility syndrome (disorder)	Finding site	Bone structure	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Familial articular hypermobility syndrome (disorder)	Finding site	Articular system structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Familial articular hypermobility syndrome (disorder)	Associated morphology	Congenital dysplasia	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Familial articular hypermobility syndrome (disorder)	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Familial articular hypermobility syndrome (disorder)	Associated morphology	Congenital dysplasia	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Familial articular hypermobility syndrome (disorder)	Finding site	Bone structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Familial articular hypermobility syndrome (disorder)	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Familial articular hypermobility syndrome (disorder)	Associated morphology	Congenital dysplasia	false	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Familial articular hypermobility syndrome (disorder)	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Familial articular hypermobility syndrome (disorder)	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Familial articular hypermobility syndrome (disorder)	Finding site	Articular system structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Familial articular hypermobility syndrome (disorder)	Pathological process (attribute)	Pathological developmental process (qualifier value)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Familial articular hypermobility syndrome (disorder)	Pathological process (attribute)	Pathological developmental process (qualifier value)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Familial articular hypermobility syndrome (disorder)	Pathological process (attribute)	Pathological developmental process (qualifier value)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Familial articular hypermobility syndrome (disorder)	Associated morphology	Dysplasia	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Familial articular hypermobility syndrome (disorder)	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Familial articular hypermobility syndrome (disorder)	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier (core metadata concept)	4
Familial articular hypermobility syndrome (disorder)	Finding site	Articular system structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	4
Familial articular hypermobility syndrome (disorder)	Associated morphology	Morphologically abnormal structure	true	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Familial articular hypermobility syndrome (disorder)	Associated morphology	Morphologically abnormal structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	4
Familial articular hypermobility syndrome (disorder)	Pathological process (attribute)	Pathological developmental process (qualifier value)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	4
Familial articular hypermobility syndrome (disorder)	Finding site	Connective tissue structure (body structure)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Familial articular hypermobility syndrome (disorder)	Is a	Skeletal dysplasia	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Familial articular hypermobility syndrome (disorder)	Is a	Autosomal dominant hereditary disorder	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Familial articular hypermobility syndrome (disorder)	Is a	Joint laxity	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Familial articular hypermobility syndrome (disorder)	Is a	Musculoskeletal and connective tissue disorder (disorder)	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Familial articular hypermobility syndrome (disorder)	Is a	Congenital connective tissue disorder	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Familial articular hypermobility syndrome (disorder)	Is a	Connective tissue hereditary disorder	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Familial articular hypermobility syndrome (disorder)	Is a	Developmental hereditary disorder	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Familial articular hypermobility syndrome (disorder)	Is a	Hereditary disorder of musculoskeletal system	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Familial articular hypermobility syndrome (disorder)	Is a	Congenital anomaly of skeletal bone	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Familial articular hypermobility syndrome (disorder)	Finding site	Joint structure	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Familial articular hypermobility syndrome (disorder)	Is a	Arthropathy	true	Inferred relationship	Existential restriction modifier (core metadata concept)

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
118471019	Ehlers-Danlos syndrome, familial joint laxity type	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
118472014	Ehlers-Danlos syndrome, type 11	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
118473016	Familial joint instability syndrome	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
118474010	Familial joint laxity	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
118475011	Familial generalized articular hypermobility	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
501851013	Familial generalised articular hypermobility	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
1233379018	Ehlers-Danlos syndrome type XI	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
5250247019	Familial articular hypermobility syndrome (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
5250248012	Familial articular hypermobility syndrome	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
118471019	Ehlers-Danlos syndrome, familial joint laxity type	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
118472014	Ehlers-Danlos syndrome, type 11	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
118473016	Familial joint instability syndrome	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
118473016	Familial joint instability syndrome	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
118474010	Familial joint laxity	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
118474010	Familial joint laxity	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
118475011	Familial generalized articular hypermobility	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
118475011	Familial generalized articular hypermobility	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
501851013	Familial generalised articular hypermobility	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
501851013	Familial generalised articular hypermobility	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
811476010	Ehlers-Danlos syndrome, familial joint laxity type (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
811476010	Ehlers-Danlos syndrome, familial joint laxity type (disorder)	en	Fully specified name	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
1233379018	Ehlers-Danlos syndrome type XI	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
1233379018	Ehlers-Danlos syndrome type XI	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
5250247019	Familial articular hypermobility syndrome (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
5250248012	Familial articular hypermobility syndrome	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3429621001000114	Gelenkhypermobilitäts-Syndrom, familiäres	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
4623371000241111	syndrome d'hypermobilité articulaire familiale	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
4623371000241111	syndrome d'hypermobilité articulaire familiale	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
3429621001000114	Gelenkhypermobilitäts-Syndrom, familiäres	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module