Spondyloenchondromatosis with basal ganglia calcification 389271000

SNOMED CT code

SNOMED code

389271000

name

Spondyloenchondromatosis with basal ganglia calcification

status

active

date introduced

2003-01-31

fully specified name(s)

Spondyloenchondromatosis with basal ganglia calcification (disorder)

synonyms

Spondyloenchondromatosis with basal ganglia calcification

attributes - group2

Finding site

Cartilage structure 771314001

Pathological process

Pathological developmental process 308490002

Occurrence

Congenital 255399007

Associated morphology

Dysplasia 25723000

attributes - group1

Finding site

Basal ganglion structure 32610002

parents

Hereditary disorder of nervous system 363235000
Spondyloenchondromatosis 389268008
Disorder of basal ganglia 70835005

hierarchies

a selection of possible paths

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Disorder of body system 362965005
Disorder of nervous system 118940003
Hereditary disorder of nervous system 363235000
Spondyloenchondromatosis with basal ganglia calcification 389271000

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Disorder of connective tissue 105969002
Connective tissue hereditary disorder 363045008
Spondyloenchondromatosis 389268008
Spondyloenchondromatosis with basal ganglia calcification 389271000

SNOMED CT Concept 138875005
Clinical finding 404684003
Finding of head and neck region 118254002
Head finding 406122000
Finding of head region 298364001
Disorder of basal ganglia 70835005
Spondyloenchondromatosis with basal ganglia calcification 389271000

ancestors

sorted most to least specific

Hereditary disorder of nervous system 363235000
Spondyloenchondromatosis 389268008
Disorder of basal ganglia 70835005
Disorganized development of cartilaginous and fibrous components of the skeleton 254140006
Finding of head region 298364001
Connective tissue hereditary disorder 363045008
Developmental hereditary disorder 363070008
Hereditary disorder of musculoskeletal system 363212003
Autosomal recessive hereditary disorder 85995004
Disorder of brain 81308009
Skeletal dysplasia 105986008
Hereditary disorder by system 363137000
Autosomal hereditary disorder 1899006
Congenital anomaly of cartilage 67988000
Disorder of head 118934005
Disorder of the central nervous system 23853001
Finding of brain 299718000
Disorder of nervous system 118940003
Congenital anomaly of musculoskeletal system 73573004
Head finding 406122000
Hereditary disease 32895009
Congenital connective tissue disorder 363039000
Cartilage disorder 50927007
Central nervous system finding 246556002
Congenital malformation 276654001
Finding of head and neck region 118254002
Genetic disease 782964007
Disorder of skeletal system 88230002
Cartilage finding 118954006
Musculoskeletal and connective tissue disorder 312225001
Developmental disorder 5294002
Disorder of connective tissue 105969002
Disorder of musculoskeletal system 928000
Congenital disease 66091009
Disorder of body system 362965005
Musculoskeletal finding 106028002
Disease 64572001
Clinical finding 404684003
SNOMED CT Concept 138875005

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SNOMED CT Concept 138875005

Clinical finding 404684003

Disease 64572001

Disorder of body system 362965005

Disorder of nervous system 118940003

Hereditary disorder of nervous system 363235000

Spondyloenchondromatosis with basal ganglia calcification 389271000

SNOMED CT code