Atypical dentin dysplasia due to SMOC2 deficiency 783059004

SNOMED CT code

SNOMED code

783059004

name

Atypical dentin dysplasia due to SMOC2 deficiency

status

active

date introduced

2019-07-31

fully specified name(s)

Atypical dentin dysplasia due to SPARC related modular calcium binding 2 deficiency (disorder)

synonyms

Atypical dentin dysplasia due to SPARC related modular calcium binding 2 deficiency
Atypical dentin dysplasia due to SMOC2 deficiency
Dentin dysplasia type 1 with microdontia and shape anomalies

attributes - group1

Finding site

Dentin structure 84540008

Associated morphology

Dysplasia 25723000

Pathological process

Pathological developmental process 308490002

Occurrence

Congenital 255399007

parents

Dentin dysplasia 109492001
Autosomal recessive hereditary disorder 85995004

hierarchies

a selection of possible paths

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Developmental disorder 5294002
Developmental hereditary disorder 363070008
Dentin dysplasia 109492001
Atypical dentin dysplasia due to SMOC2 deficiency 783059004

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Genetic disease 782964007
Hereditary disease 32895009
Autosomal hereditary disorder 1899006
Autosomal recessive hereditary disorder 85995004
Atypical dentin dysplasia due to SMOC2 deficiency 783059004

ancestors

sorted most to least specific

Dentin dysplasia 109492001
Autosomal recessive hereditary disorder 85995004
Oral lesion 1071000119107
Autosomal dominant hereditary disorder 11164009
Hereditary disorder of tooth 1148766007
Developmental hereditary disorder 363070008
Congenital anomaly of tooth 422977003
Disorder of hard tissues of teeth 46557008
Autosomal hereditary disorder 1899006
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
Hereditary disease 32895009
Tooth disorder 234947003
Congenital anomaly of head 87290003
Congenital malformation of upper alimentary tract 275262008
Genetic disease 782964007
Disorder of teeth AND/OR supporting structures 105995000
Tooth finding 278544002
Disorder of digestive organ 76712006
Congenital anomaly of digestive tract 95470009
Disease of mouth 118938008
Oral cavity finding 116337000
Congenital anomaly of digestive system 69518005
Disorder of jaw 37156001
Disorder of head 118934005
Finding of mouth region 423066003
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
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

Disease 64572001

Developmental disorder 5294002

Developmental hereditary disorder 363070008

Dentin dysplasia 109492001

Atypical dentin dysplasia due to SMOC2 deficiency 783059004

SNOMED CT code