Amelogenesis imperfecta and gingival hyperplasia syndrome 707607008

SNOMED CT code

SNOMED code

707607008

name

Amelogenesis imperfecta and gingival hyperplasia syndrome

status

active

date introduced

2015-01-31

fully specified name(s)

Amelogenesis imperfecta and gingival hyperplasia syndrome (disorder)

synonyms

Amelogenesis imperfecta and gingival hyperplasia syndrome

attributes - group1

Associated morphology

Hyperplasia 76197007

Finding site

Gingival structure 113279002

Pathological process

Pathological developmental process 308490002

Occurrence

Congenital 255399007

attributes - group2

Pathological process

Pathological developmental process 308490002

Associated morphology

Morphologically abnormal structure 49755003

Finding site

Enamel structure 76993005

Occurrence

Congenital 255399007

parents

Hyperplasia of gingiva 441798003
Amelogenesis imperfecta 78494001
Autosomal recessive hereditary disorder 85995004

hierarchies

a selection of possible paths

SNOMED CT Concept 138875005
Clinical finding 404684003
General finding of soft tissue 248402002
Gingivae finding 249410009
Gingival disease 18718003
Hyperplasia of gingiva 441798003
Amelogenesis imperfecta and gingival hyperplasia syndrome 707607008

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Developmental disorder 5294002
Developmental hereditary disorder 363070008
Amelogenesis imperfecta 78494001
Amelogenesis imperfecta and gingival hyperplasia syndrome 707607008

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Genetic disease 782964007
Hereditary disease 32895009
Autosomal hereditary disorder 1899006
Autosomal recessive hereditary disorder 85995004
Amelogenesis imperfecta and gingival hyperplasia syndrome 707607008

ancestors

sorted most to least specific

Hyperplasia of gingiva 441798003
Amelogenesis imperfecta 78494001
Autosomal recessive hereditary disorder 85995004
Gingival disease 18718003
Hereditary disorder of tooth 1148766007
Autosomal hereditary disorder 1899006
Developmental hereditary disorder 363070008
Congenital anomaly of tooth 422977003
Disorder of hard tissues of teeth 46557008
Gingivae finding 249410009
Periodontal disease 2556008
Disorder of oral soft tissues 41188003
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 soft tissue of head 280131007
Disorder of tooth development 371136004
Congenital anomaly of mouth 128334002
Tooth disorder 234947003
Hereditary disease 32895009
Disorder of soft tissue 19660004
Congenital anomaly of head 87290003
Congenital malformation of upper alimentary tract 275262008
Disorder of teeth AND/OR supporting structures 105995000
Genetic disease 782964007
General finding of soft tissue 248402002
Tooth finding 278544002
Disorder of digestive organ 76712006
Congenital anomaly of digestive tract 95470009
Oral cavity finding 116337000
Disease of mouth 118938008
Congenital anomaly of digestive system 69518005
Disorder of jaw 37156001
Finding of mouth region 423066003
Disorder of head 118934005
Congenital malformation 276654001
Disorder of upper digestive tract 50410009
Finding of head region 298364001
Developmental disorder 5294002
Disorder of digestive tract 84410009
Congenital disease 66091009
Head finding 406122000
Disorder of digestive system 53619000
Finding of head and neck region 118254002
Digestive system finding 386617003
Disorder of body system 362965005
Disease 64572001
Clinical finding 404684003
SNOMED CT Concept 138875005

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SNOMED CT Concept 138875005

Clinical finding 404684003

General finding of soft tissue 248402002

Gingivae finding 249410009

Gingival disease 18718003

Hyperplasia of gingiva 441798003

Amelogenesis imperfecta and gingival hyperplasia syndrome 707607008

SNOMED CT code