Congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration 715436007

SNOMED CT code

SNOMED code

715436007

name

Congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration

status

active

date introduced

2016-07-31

fully specified name(s)

Congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration (disorder)

synonyms

Congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration
Cerebellar hypoplasia and tapetoretinal degeneration

attributes - group2

Finding site

Visual structure 49549006

Pathological process

Pathological developmental process 308490002

attributes - group1

Associated morphology

Hypoplasia 55199003

Finding site

Cerebellar structure 113305005

Pathological process

Pathological developmental process 308490002

Occurrence

Congenital 255399007

parents

Congenital cerebellar hypoplasia 16026008
Developmental hereditary disorder 363070008
Hereditary disorder of nervous system 363235000
Hereditary disorder of the visual system 363343008

hierarchies

a selection of possible paths

SNOMED CT Concept 138875005
Clinical finding 404684003
Central nervous system finding 246556002
Finding of brain 299718000
Disorder of brain 81308009
Cerebellar disorder 223176004
Dysgenesis of the cerebellum 253171007
Congenital cerebellar hypoplasia 16026008
Congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration 715436007

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Developmental disorder 5294002
Developmental hereditary disorder 363070008
Congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration 715436007

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
Congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration 715436007

SNOMED CT Concept 138875005
Clinical finding 404684003
Eye / vision finding 118235002
Visual system disorder 128127008
Hereditary disorder of the visual system 363343008
Congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration 715436007

ancestors

sorted most to least specific

Congenital cerebellar hypoplasia 16026008
Developmental hereditary disorder 363070008
Hereditary disorder of nervous system 363235000
Hereditary disorder of the visual system 363343008
Dysgenesis of the cerebellum 253171007
Visual system disorder 128127008
Congenital hypoplasia of part of brain 78693004
Hereditary disorder by system 363137000
Cerebellar disorder 223176004
Hereditary disease 32895009
Eye / vision finding 118235002
Congenital hypoplasia of brain 127551000119100
Genetic disease 782964007
Congenital anomaly of brain 57148006
Disorder of brain 81308009
Congenital anomaly of central nervous system 128124001
Congenital anomaly of head 87290003
Disorder of head 118934005
Disorder of the central nervous system 23853001
Finding of brain 299718000
Congenital anomaly of nervous system 88425004
Head finding 406122000
Disorder of nervous system 118940003
Central nervous system finding 246556002
Congenital malformation 276654001
Finding of head and neck region 118254002
Disorder of body system 362965005
Developmental disorder 5294002
Congenital disease 66091009
Disease 64572001
Clinical finding 404684003
SNOMED CT Concept 138875005

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SNOMED CT Concept 138875005

Clinical finding 404684003

Central nervous system finding 246556002

Finding of brain 299718000

Disorder of brain 81308009

Cerebellar disorder 223176004

Dysgenesis of the cerebellum 253171007

Congenital cerebellar hypoplasia 16026008

Congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration 715436007

SNOMED CT code