Progressive bifocal chorioretinal atrophy 719266007

SNOMED CT code

SNOMED code

719266007

name

Progressive bifocal chorioretinal atrophy

status

active

date introduced

2017-01-31

fully specified name(s)

Progressive bifocal chorioretinal atrophy (disorder)

synonyms

Progressive bifocal chorioretinal atrophy

attributes - group2

Associated morphology

Dystrophy 4720007

Finding site

Retinal structure 5665001

attributes - group3

Associated morphology

Dystrophy 4720007

Finding site

Choroidal structure 68703001

parents

Autosomal dominant hereditary disorder 11164009
Chorioretinal degeneration 247177004
Hereditary retinal dystrophy 41799005

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
Progressive bifocal chorioretinal atrophy 719266007

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Degenerative disorder 362975008
Degenerative disorder of eye 62585004
Choroidal degeneration 406446000
Chorioretinal degeneration 247177004
Progressive bifocal chorioretinal atrophy 719266007

SNOMED CT Concept 138875005
Clinical finding 404684003
Eye / vision finding 118235002
Visual system disorder 128127008
Hereditary disorder of the visual system 363343008
Hereditary retinal dystrophy 41799005
Progressive bifocal chorioretinal atrophy 719266007

ancestors

sorted most to least specific

Autosomal dominant hereditary disorder 11164009
Chorioretinal degeneration 247177004
Hereditary retinal dystrophy 41799005
Autosomal hereditary disorder 1899006
Chorioretinal disorder 302893000
Retinal dystrophy 314407005
Choroidal degeneration 406446000
Hereditary disorder of the visual system 363343008
Disorder of choroid of eye 128468007
Degeneration of retina 95695004
Retina and choroid finding 247103004
Hereditary disorder by system 363137000
Hereditary disease 32895009
Retinal disorder 29555009
Choroid finding 247195001
Disorder of uveal tract 95678007
Degenerative disorder of eye 62585004
Genetic disease 782964007
Disorder of vitreous body and retina 312771007
Anomaly of eye 11131000119108
Retina finding 399858007
Degenerative disorder 362975008
Disorder of posterior segment of eye 128536001
Disorder of eye 371405004
Disorder of sensory organ 1279550006
Globe finding 246915008
Disorder of eye region 371409005
Disorder of head 118934005
Visual system disorder 128127008
Finding of head region 298364001
Eye / vision finding 118235002
Head finding 406122000
Disorder of body system 362965005
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

Progressive bifocal chorioretinal atrophy 719266007

SNOMED CT code