Amelogenesis imperfecta 78494001

SNOMED CT code

SNOMED code

78494001

name

Amelogenesis imperfecta

status

active

date introduced

2002-01-31

fully specified name(s)

Amelogenesis imperfecta (disorder)

synonyms

Amelogenesis imperfecta
Congenital enamel hypoplasia
AI - Amelogenesis imperfecta

attributes - group1

Associated morphology

Morphologically abnormal structure 49755003

Pathological process

Pathological developmental process 308490002

Finding site

Enamel structure 76993005

Occurrence

Congenital 255399007

parents

Hereditary disorder of tooth 1148766007
Developmental hereditary disorder 363070008
Congenital anomaly of tooth 422977003
Disorder of hard tissues of teeth 46557008

children

Agenesis of enamel 699382004
Amelogenesis imperfecta and gingival hyperplasia syndrome 707607008
Amelogenesis imperfecta co-occurrent with cone rod dystrophy 707608003
Amelogenesis imperfecta, hypocalcification type 109471001
Amelogenesis imperfecta, hypomaturation type 109475005
Amelogenesis imperfecta, hypoplastic type 109476006
Ectodermal dysplasia, hyperhidrosis, cutaneous syndactyly syndrome 1279835008
Enamel-renal syndrome 109477002
Kohlschutter's syndrome 109478007
Late-onset localized junctional epidermolysis bullosa, intellectual disability syndrome 773692000
Short stature, unique facies, enamel hypoplasia, progressive joint stiffness, high-pitched voice syndrome 726672000
Stimmler syndrome 733072002
Trichodysplasia with amelogenesis imperfecta syndrome 719911000
Verloes Bourguignon syndrome 716195006

hierarchies

a selection of possible paths

SNOMED CT Concept 138875005
Clinical finding 404684003
Digestive system finding 386617003
Disorder of digestive system 53619000
Digestive system hereditary disorder 363080007
Hereditary disorder of tooth 1148766007
Amelogenesis imperfecta 78494001

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Developmental disorder 5294002
Developmental hereditary disorder 363070008
Amelogenesis imperfecta 78494001

SNOMED CT Concept 138875005
Clinical finding 404684003
Digestive system finding 386617003
Finding of mouth region 423066003
Oral cavity finding 116337000
Congenital abnormality of oral cavity 282041002
Congenital anomaly of tooth 422977003
Amelogenesis imperfecta 78494001

SNOMED CT Concept 138875005
Clinical finding 404684003
Digestive system finding 386617003
Disorder of digestive system 53619000
Disorder of digestive organ 76712006
Tooth disorder 234947003
Disorder of hard tissues of teeth 46557008
Amelogenesis imperfecta 78494001

ancestors

sorted most to least specific

Hereditary disorder of tooth 1148766007
Developmental hereditary disorder 363070008
Congenital anomaly of tooth 422977003
Disorder of hard tissues of teeth 46557008
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
Hereditary disorder by system 363137000
Disorder of tooth development 371136004
Congenital anomaly of mouth 128334002
Tooth disorder 234947003
Hereditary disease 32895009
Congenital anomaly of head 87290003
Congenital malformation of upper alimentary tract 275262008
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
Oral cavity finding 116337000
Congenital anomaly of digestive system 69518005
Disease of mouth 118938008
Disorder of jaw 37156001
Finding of mouth region 423066003
Congenital malformation 276654001
Disorder of head 118934005
Disorder of upper digestive tract 50410009
Finding of head region 298364001
Developmental disorder 5294002
Congenital disease 66091009
Disorder of digestive tract 84410009
Head finding 406122000
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

Digestive system finding 386617003

Disorder of digestive system 53619000

Digestive system hereditary disorder 363080007

Hereditary disorder of tooth 1148766007

Amelogenesis imperfecta 78494001

SNOMED CT code