Oculodentodigital syndrome 38215007

SNOMED CT code

SNOMED code

38215007

name

Oculodentodigital syndrome

status

active

date introduced

2002-01-31

fully specified name(s)

Oculodentodigital syndrome (disorder)

synonyms

Curtius' syndrome I
Oculodentodigital syndrome
Oculodentodigital dysplasia

attributes - group4

Finding site

Ectoderm structure 63206006

Pathological process

Pathological developmental process 308490002

Occurrence

Congenital 255399007

Associated morphology

Dysplasia 25723000

attributes - group2

Pathological process

Pathological developmental process 308490002

Associated morphology

Morphologically abnormal structure 49755003

Finding site

Limb structure 66019005

Occurrence

Congenital 255399007

attributes - group3

Associated morphology

Morphologically abnormal structure 49755003

Occurrence

Congenital 255399007

Finding site

Face structure 89545001

Pathological process

Pathological developmental process 308490002

attributes - group1

Pathological process

Pathological developmental process 308490002

Occurrence

Congenital 255399007

Finding site

Skin structure 39937001

Associated morphology

Dysplasia 25723000

attributes - group5

Finding site

Hair structure 386045008

Pathological process

Pathological developmental process 308490002

Associated morphology

Morphologically abnormal structure 49755003

Occurrence

Congenital 255399007

attributes - group6

Associated morphology

Morphologically abnormal structure 49755003

Finding site

Tooth structure 38199008

Pathological process

Pathological developmental process 308490002

Occurrence

Congenital 255399007

parents

Multiple malformation syndrome with facial-limb defects as major feature 23359005
Ectodermal dysplasia with hair-tooth defects 239027006
Skin lesion 95324001

hierarchies

a selection of possible paths

SNOMED CT Concept 138875005
Clinical finding 404684003
Finding of limb structure 302293008
Disorder of limb 128605003
Congenital anomaly of limb 60475009
Multiple malformation syndrome with facial-limb defects as major feature 23359005
Oculodentodigital syndrome 38215007

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Disorder of embryonic structure 609521009
Congenital ectodermal defect 254154003
Ectodermal dysplasia 8654005
Ectodermal dysplasia with hair-tooth defects 239027006
Oculodentodigital syndrome 38215007

SNOMED CT Concept 138875005
Clinical finding 404684003
General finding of soft tissue 248402002
Disorder of soft tissue 19660004
Soft tissue lesion 239953001
Skin lesion 95324001
Oculodentodigital syndrome 38215007

ancestors

sorted most to least specific

Multiple malformation syndrome with facial-limb defects as major feature 23359005
Ectodermal dysplasia with hair-tooth defects 239027006
Skin lesion 95324001
Multiple malformation syndrome with limb defect as major feature 41443008
Congenital anomaly of tooth 422977003
Soft tissue lesion 239953001
Congenital anomaly of limb 60475009
Multiple malformation syndrome with facial defects as major feature 65094009
Congenital anomaly of hair 65033000
Ectodermal dysplasia 8654005
Lesion of skin and/or skin-associated mucous membrane 714974000
Multiple system malformation syndrome 82354003
Congenital anomaly of digestive organ 128332003
Disorder of limb 128605003
Congenital anomaly of face 398302004
Genodermatosis 239001006
Congenital abnormality of oral cavity 282041002
Malformation of tooth 422775003
Congenital anomaly of jaw 95473006
Skin or mucosa lesion 247440002
Disorder of hair 279425004
Congenital ectodermal defect 254154003
Congenital malformation syndrome 400038003
Finding of limb structure 302293008
Disorder of face 118930001
Congenital anomaly of skin 199879009
Disorder of tooth development 371136004
Disorder of skin appendage 238714008
Congenital anomaly of mouth 128334002
Hair finding 247522004
Disorder of embryonic structure 609521009
Congenital anomaly of integument 38164009
Tooth disorder 234947003
Disorder of skin 95320005
Congenital anomaly of head 87290003
Finding of face 301310005
Congenital malformation of upper alimentary tract 275262008
Disorder of teeth AND/OR supporting structures 105995000
Disorder of digestive organ 76712006
Skin finding 106076001
Tooth finding 278544002
Disorder of skin and/or subcutaneous tissue 80659006
Congenital anomaly of digestive tract 95470009
Congenital anomaly of digestive system 69518005
Disorder of soft tissue 19660004
Disorder of integument 128598002
Oral cavity finding 116337000
Disorder of jaw 37156001
Disease of mouth 118938008
Skin AND/OR mucosa finding 415531008
Congenital malformation 276654001
General finding of soft tissue 248402002
Disorder of head 118934005
Integumentary system finding 106077005
Finding of mouth region 423066003
Disorder of upper digestive tract 50410009
Developmental disorder 5294002
Congenital disease 66091009
Finding of head region 298364001
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

Finding of limb structure 302293008

Disorder of limb 128605003

Congenital anomaly of limb 60475009

Multiple malformation syndrome with facial-limb defects as major feature 23359005

Oculodentodigital syndrome 38215007

SNOMED CT code