Amelogenesis imperfecta co-occurrent with cone rod dystrophy 707608003

SNOMED CT code

SNOMED code

707608003

name

Amelogenesis imperfecta co-occurrent with cone rod dystrophy

status

active

date introduced

2015-01-31

fully specified name(s)

Amelogenesis imperfecta co-occurrent with cone rod dystrophy (disorder)

synonyms

Jalili syndrome
Amelogenesis imperfecta co-occurrent with cone rod dystrophy

attributes - group1

Occurrence

Congenital 255399007

Pathological process

Pathological developmental process 308490002

Associated morphology

Morphologically abnormal structure 49755003

Finding site

Enamel structure 76993005

attributes - group2

Associated morphology

Dystrophy 4720007

Finding site

Retinal structure 5665001

parents

Hereditary retinal dystrophy 41799005
Amelogenesis imperfecta 78494001

hierarchies

a selection of possible paths

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
Amelogenesis imperfecta co-occurrent with cone rod dystrophy 707608003

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Developmental disorder 5294002
Developmental hereditary disorder 363070008
Amelogenesis imperfecta 78494001
Amelogenesis imperfecta co-occurrent with cone rod dystrophy 707608003

ancestors

sorted most to least specific

Hereditary retinal dystrophy 41799005
Amelogenesis imperfecta 78494001
Retinal dystrophy 314407005
Hereditary disorder of tooth 1148766007
Hereditary disorder of the visual system 363343008
Developmental hereditary disorder 363070008
Congenital anomaly of tooth 422977003
Disorder of hard tissues of teeth 46557008
Degeneration of retina 95695004
Congenital anomaly of digestive organ 128332003
Digestive system hereditary disorder 363080007
Congenital abnormality of oral cavity 282041002
Malformation of tooth 422775003
Congenital anomaly of jaw 95473006
Retinal disorder 29555009
Degenerative disorder of eye 62585004
Hereditary disorder by system 363137000
Disorder of tooth development 371136004
Congenital anomaly of mouth 128334002
Disorder of vitreous body and retina 312771007
Tooth disorder 234947003
Anomaly of eye 11131000119108
Retina finding 399858007
Hereditary disease 32895009
Degenerative disorder 362975008
Congenital anomaly of head 87290003
Congenital malformation of upper alimentary tract 275262008
Disorder of posterior segment of eye 128536001
Disorder of teeth AND/OR supporting structures 105995000
Genetic disease 782964007
Tooth finding 278544002
Disorder of digestive organ 76712006
Congenital anomaly of digestive tract 95470009
Disorder of eye 371405004
Oral cavity finding 116337000
Congenital anomaly of digestive system 69518005
Disease of mouth 118938008
Disorder of jaw 37156001
Disorder of sensory organ 1279550006
Finding of mouth region 423066003
Globe finding 246915008
Disorder of eye region 371409005
Congenital malformation 276654001
Disorder of upper digestive tract 50410009
Finding of head region 298364001
Visual system disorder 128127008
Disorder of head 118934005
Developmental disorder 5294002
Congenital disease 66091009
Disorder of digestive tract 84410009
Head finding 406122000
Eye / vision finding 118235002
Disorder of digestive system 53619000
Finding of head and neck region 118254002
Disorder of body system 362965005
Digestive system finding 386617003
Disease 64572001
Clinical finding 404684003
SNOMED CT Concept 138875005

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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

Amelogenesis imperfecta co-occurrent with cone rod dystrophy 707608003

SNOMED CT code