Spastic paraplegia with Paget disease of bone syndrome 726622002

SNOMED CT code

SNOMED code

726622002

name

Spastic paraplegia with Paget disease of bone syndrome

status

active

date introduced

2017-07-31

fully specified name(s)

Spastic paraplegia with Paget disease of bone syndrome (disorder)

synonyms

Spastic paraplegia with Paget disease of bone syndrome

attributes - group2

Clinical course

Progressive 255314001

attributes - group4

Associated morphology

Degenerative abnormality 107669003

Finding site

Spinal cord structure 2748008

attributes - group7

Interprets

Movement 255324009

attributes - group5

Finding site

Right lower extremity structure 62175007

attributes - group6

Finding site

Left lower extremity structure 32153003

attributes - group1

Interprets

Movement observable 363847004

Has interpretation

Absent 2667000

attributes - group3

Finding site

Bone structure 272673000

parents

Autosomal dominant complex hereditary spastic paraplegia 1259038005
Chronic disease of musculoskeletal system 128237006
Osteitis deformans 2089002
Hereditary disorder of musculoskeletal system 363212003

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
Autosomal dominant hereditary disorder 11164009
Autosomal dominant hereditary spastic paraplegia 737227004
Autosomal dominant complex hereditary spastic paraplegia 1259038005
Spastic paraplegia with Paget disease of bone syndrome 726622002

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Chronic disease 27624003
Chronic disease of musculoskeletal system 128237006
Spastic paraplegia with Paget disease of bone syndrome 726622002

SNOMED CT Concept 138875005
Clinical finding 404684003
Musculoskeletal finding 106028002
Bone finding 118953000
Disorder of bone 76069003
Osteitis deformans 2089002
Spastic paraplegia with Paget disease of bone syndrome 726622002

SNOMED CT Concept 138875005
Clinical finding 404684003
Musculoskeletal finding 106028002
Disorder of musculoskeletal system 928000
Hereditary disorder of musculoskeletal system 363212003
Spastic paraplegia with Paget disease of bone syndrome 726622002

ancestors

sorted most to least specific

Autosomal dominant complex hereditary spastic paraplegia 1259038005
Chronic disease of musculoskeletal system 128237006
Osteitis deformans 2089002
Hereditary disorder of musculoskeletal system 363212003
Complicated hereditary spastic paraplegia 230261006
Disorder of bone 76069003
Autosomal dominant hereditary spastic paraplegia 737227004
Hereditary spastic paraplegia 39912006
Bone finding 118953000
Autosomal dominant hereditary disorder 11164009
Disorder of skeletal system 88230002
Hereditary degenerative disease of central nervous system 106018006
Autosomal hereditary disorder 1899006
Spastic paraplegia 192967009
Chronic myelopathy 434371000124108
Chronic paraplegia 698292000
Disorder of musculoskeletal system 928000
Hereditary disorder of nervous system 363235000
Musculoskeletal finding 106028002
Spastic syndrome 386781001
Chronic nervous system disorder 128283000
Degenerative disease of the central nervous system 80690008
Paraplegia 60389000
Myelopathy 48522003
Chronic disease 27624003
Hereditary disorder by system 363137000
Disorder of the central nervous system 23853001
Complete bilateral paralysis 29188005
Degenerative disorder 362975008
Bilateral lower limb paralytic syndrome 609553000
Finding of spinal cord 299733008
Disorder of spinal region 410730009
Disorder of nervous system 118940003
Hereditary disease 32895009
Central nervous system finding 246556002
Paralytic syndrome 29426003
Finding of spinal region 298379008
Disorder of right lower extremity 451421000124102
Disorder of left lower extremity 451431000124104
Disorder of back 33308003
Disorder of body system 362965005
Genetic disease 782964007
Paralysis 44695005
Finding of back 414252009
Disorder of lower limb 118937003
Movement disorder 60342002
Motor dysfunction 52559000
Finding of lower limb 116312005
Disorder of limb 128605003
Disease 64572001
Motor nervous system finding 106145009
Finding of limb structure 302293008
Finding of movement 298325004
Neurological finding 102957003
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

Autosomal dominant hereditary disorder 11164009

Autosomal dominant hereditary spastic paraplegia 737227004

Autosomal dominant complex hereditary spastic paraplegia 1259038005

Spastic paraplegia with Paget disease of bone syndrome 726622002

SNOMED CT code