Helicoid peripapillary chorioretinal degeneration 724384008

SNOMED CT code

SNOMED code

724384008

name

Helicoid peripapillary chorioretinal degeneration

status

active

date introduced

2017-07-31

fully specified name(s)

Helicoid peripapillary chorioretinal degeneration (disorder)

synonyms

Helicoid peripapillary chorioretinal degeneration
Atrophia areata
Sveinsson chorioretinal atrophy

attributes - group2

Associated morphology

Atrophy 13331008

Finding site

Peripapillary retina 280615000

attributes - group3

Associated morphology

Atrophy 13331008

Finding site

Peripapillary choroid 423914005

parents

Autosomal dominant hereditary disorder 11164009
Hereditary disorder of the visual system 363343008
Peripapillary atrophy 420535003
Chorioretinal atrophy 95686007

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
Helicoid peripapillary chorioretinal degeneration 724384008

SNOMED CT Concept 138875005
Clinical finding 404684003
Eye / vision finding 118235002
Visual system disorder 128127008
Hereditary disorder of the visual system 363343008
Helicoid peripapillary chorioretinal degeneration 724384008

SNOMED CT Concept 138875005
Clinical finding 404684003
Eye / vision finding 118235002
Globe finding 246915008
Retina finding 399858007
Peripapillary atrophy 420535003
Helicoid peripapillary chorioretinal degeneration 724384008

SNOMED CT Concept 138875005
Clinical finding 404684003
Eye / vision finding 118235002
Globe finding 246915008
Choroid finding 247195001
Choroidal atrophy 247200005
Chorioretinal atrophy 95686007
Helicoid peripapillary chorioretinal degeneration 724384008

ancestors

sorted most to least specific

Autosomal dominant hereditary disorder 11164009
Hereditary disorder of the visual system 363343008
Peripapillary atrophy 420535003
Chorioretinal atrophy 95686007
Autosomal hereditary disorder 1899006
Chorioretinal degeneration 247177004
Hereditary disorder by system 363137000
Choroidal atrophy 247200005
Atrophic retina 405722004
Hereditary disease 32895009
Chorioretinal disorder 302893000
Atrophy of globe of eye 1229938006
Choroidal degeneration 406446000
Degeneration of retina 95695004
Genetic disease 782964007
Disorder of choroid of eye 128468007
Degenerative disorder of eye 62585004
Retinal disorder 29555009
Retina and choroid finding 247103004
Retina finding 399858007
Choroid finding 247195001
Anomaly of eye 11131000119108
Disorder of vitreous body and retina 312771007
Disorder of uveal tract 95678007
Degenerative disorder 362975008
Disorder of posterior segment of eye 128536001
Disorder of eye 371405004
Globe finding 246915008
Disorder of sensory organ 1279550006
Disorder of eye region 371409005
Visual system disorder 128127008
Finding of head region 298364001
Disorder of head 118934005
Eye / vision finding 118235002
Disorder of body system 362965005
Head finding 406122000
Disease 64572001
Finding of head and neck region 118254002
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

Helicoid peripapillary chorioretinal degeneration 724384008

SNOMED CT code