Congenital hereditary endothelial dystrophy type 1 416633008

SNOMED CT code

SNOMED code

416633008

name

Congenital hereditary endothelial dystrophy type 1

status

active

date introduced

2005-07-31

fully specified name(s)

Congenital hereditary endothelial dystrophy type 1 (disorder)

synonyms

Congenital hereditary endothelial dystrophy autosomal dominant form
Congenital hereditary endothelial dystrophy type 1
CHED1 - congenital hereditary endothelial dystrophy type 1

attributes - group2

Pathological process

Pathological developmental process 308490002

Occurrence

Congenital 255399007

Finding site

Chromosome pair 20 25610001

Associated morphology

Cellular AND/OR subcellular abnormality 107673000

attributes - group1

Associated morphology

Dystrophy 4720007

Finding site

Structure of corneal endothelium 65431007

parents

Autosomal dominant hereditary disorder 11164009
Congenital hereditary endothelial dystrophy 417651000

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
Congenital hereditary endothelial dystrophy type 1 416633008

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Developmental disorder 5294002
Congenital malformation 276654001
Congenital hereditary endothelial dystrophy 417651000
Congenital hereditary endothelial dystrophy type 1 416633008

ancestors

sorted most to least specific

Autosomal dominant hereditary disorder 11164009
Congenital hereditary endothelial dystrophy 417651000
Autosomal hereditary disorder 1899006
Congenital malformation 276654001
Developmental hereditary disorder 363070008
Corneal endothelial dystrophy 416960004
Hereditary corneal dystrophy 77797009
Anomaly of chromosome pair 20 9839007
Developmental disorder 5294002
Corneal endothelium finding 246966003
Hereditary disorder of the visual system 363343008
Anomaly of chromosome pair 362984008
Posterior corneal dystrophy 35091000119101
Congenital chromosomal disease 74345006
Corneal dystrophy 5587004
Hereditary disorder by system 363137000
Hereditary disease 32895009
Chromosomal disorder 409709004
Congenital disease 66091009
Corneal degeneration 111521006
Genetic disease 782964007
Disorder of cornea 15250008
Degenerative disorder of eye 62585004
Corneal finding 246924004
Disorder of anterior segment of eye 128535002
Anomaly of eye 11131000119108
Degenerative disorder 362975008
Anterior segment finding 418727003
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
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

Congenital hereditary endothelial dystrophy type 1 416633008

SNOMED CT code