Hypermobile Ehlers-Danlos syndrome 30652003

SNOMED CT code

SNOMED code

30652003

name

Hypermobile Ehlers-Danlos syndrome

status

active

date introduced

2002-01-31

fully specified name(s)

Hypermobile Ehlers-Danlos syndrome (disorder)

synonyms

Ehlers-Danlos syndrome type III
Ehlers-Danlos syndrome, type 3
Benign hypermobility syndrome
Ehlers-Danlos syndrome, benign hypermobile form
Hypermobile Ehlers-Danlos syndrome

attributes - group3

Pathological process

Pathological developmental process 308490002

Associated morphology

Dysplasia 25723000

Finding site

Joint structure 39352004

Occurrence

Congenital 255399007

attributes - group1

Pathological process

Pathological developmental process 308490002

Occurrence

Congenital 255399007

Finding site

Bone structure 272673000

Associated morphology

Dysplasia 25723000

attributes - group2

Pathological process

Pathological developmental process 308490002

Associated morphology

Dysplasia 25723000

Occurrence

Congenital 255399007

Finding site

Skin structure 39937001

attributes - group4

Associated morphology

Dysplasia 25723000

Pathological process

Pathological developmental process 308490002

Finding site

Skeletal ligament structure 410743009

Occurrence

Congenital 255399007

attributes - group5

Interprets

Range of joint movement 364564000

Has interpretation

Above reference range 281302008

attributes - group6

Finding site

Structure of ligament of joint 123859001

parents

Autosomal hereditary disorder 1899006
Congenital anomaly of bone and joint 237513002
Lesion of joint 298149009
Ehlers-Danlos syndrome 398114001
Hypermobility syndrome 85551004

hierarchies

a selection of possible paths

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Genetic disease 782964007
Hereditary disease 32895009
Autosomal hereditary disorder 1899006
Hypermobile Ehlers-Danlos syndrome 30652003

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Developmental disorder 5294002
Disorder of bone development 371521007
Congenital anomaly of skeletal bone 8447006
Congenital anomaly of bone and joint 237513002
Hypermobile Ehlers-Danlos syndrome 30652003

SNOMED CT Concept 138875005
Clinical finding 404684003
Musculoskeletal finding 106028002
Joint finding 118952005
Arthropathy 399269003
Lesion of joint 298149009
Hypermobile Ehlers-Danlos syndrome 30652003

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Disorder of connective tissue 105969002
Musculoskeletal and connective tissue disorder 312225001
Ehlers-Danlos syndrome 398114001
Hypermobile Ehlers-Danlos syndrome 30652003

SNOMED CT Concept 138875005
Clinical finding 404684003
Finding of movement 298325004
Movement disorder 60342002
Hypermobility syndrome 85551004
Hypermobile Ehlers-Danlos syndrome 30652003

ancestors

sorted most to least specific

Autosomal hereditary disorder 1899006
Congenital anomaly of bone and joint 237513002
Lesion of joint 298149009
Ehlers-Danlos syndrome 398114001
Hypermobility syndrome 85551004
Congenital anomaly of skeletal bone 8447006
Skeletal dysplasia 105986008
Laxity of ligament 27911000
Congenital anomaly of joint 95463009
Congenital anomaly of skin 199879009
Congenital connective tissue disorder 363039000
Connective tissue hereditary disorder 363045008
Developmental hereditary disorder 363070008
Hereditary disorder of the integument 363185004
Hereditary disorder of musculoskeletal system 363212003
Metabolic bone disease 50279003
Metabolic disease of collagen 73873008
Skin lesion 95324001
Movement disorder 60342002
Hypermobility of joint 788453008
Disorder of bone development 371521007
Arthropathy 399269003
Congenital anomaly of musculoskeletal system 73573004
Disorder of ligament 60492000
Congenital anomaly of integument 38164009
Hereditary disorder by system 363137000
Metabolic disease 75934005
Soft tissue lesion 239953001
Disorder of skin 95320005
Lesion of skin and/or skin-associated mucous membrane 714974000
Range of joint movement increased 298181000
Hereditary disease 32895009
Joint finding 118952005
Congenital malformation 276654001
Disorder of bone 76069003
Disorder of joint region 785875003
Musculoskeletal and connective tissue disorder 312225001
Ligament finding 250132005
Skin finding 106076001
Skin or mucosa lesion 247440002
Finding of range of joint movement 298180004
Disorder of skin and/or subcutaneous tissue 80659006
Genetic disease 782964007
Developmental disorder 5294002
Disorder of soft tissue 19660004
Bone finding 118953000
Disorder of skeletal system 88230002
Disorder of integument 128598002
Disorder of connective tissue 105969002
Congenital disease 66091009
Finding of joint movement 298179002
Skin AND/OR mucosa finding 415531008
General finding of soft tissue 248402002
Disorder of musculoskeletal system 928000
Integumentary system finding 106077005
Finding of movement 298325004
Musculoskeletal finding 106028002
Disorder of body system 362965005
Disease 64572001
Clinical finding 404684003
SNOMED CT Concept 138875005

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SNOMED CT Concept 138875005

Clinical finding 404684003

Disease 64572001

Genetic disease 782964007

Hereditary disease 32895009

Autosomal hereditary disorder 1899006

Hypermobile Ehlers-Danlos syndrome 30652003

SNOMED CT code