Cranioectodermal dysplasia 254093009

SNOMED CT code

SNOMED code

254093009

name

Cranioectodermal dysplasia

status

active

date introduced

2002-01-31

fully specified name(s)

Cranioectodermal dysplasia (disorder)

synonyms

Cranioectodermal dysplasia
Sensenbrenner's syndrome

attributes - group1

Pathological process

Pathological developmental process 308490002

Occurrence

Congenital 255399007

Finding site

Bone structure 272673000

Associated morphology

Dysplasia 25723000

attributes - group3

Associated morphology

Morphologically abnormal structure 49755003

Pathological process

Pathological developmental process 308490002

Finding site

Hair structure 386045008

Occurrence

Congenital 255399007

attributes - group2

Pathological process

Pathological developmental process 308490002

Finding site

Ectoderm structure 63206006

Occurrence

Congenital 255399007

Associated morphology

Dysplasia 25723000

attributes - group4

Finding site

Tooth structure 38199008

Pathological process

Pathological developmental process 308490002

Associated morphology

Morphologically abnormal structure 49755003

Occurrence

Congenital 255399007

parents

Ectodermal dysplasia with hair-tooth defects 239027006
Acromesomelic dysplasia syndrome 279082008

hierarchies

a selection of possible paths

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
Cranioectodermal dysplasia 254093009

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Developmental disorder 5294002
Disorder of bone development 371521007
Congenital anomaly of skeletal bone 8447006
Acromesomelic dysplasia syndrome 279082008
Cranioectodermal dysplasia 254093009

ancestors

sorted most to least specific

Ectodermal dysplasia with hair-tooth defects 239027006
Acromesomelic dysplasia syndrome 279082008
Congenital anomaly of tooth 422977003
Skeletal dysplasia 105986008
Congenital anomaly of hair 65033000
Ectodermal dysplasia 8654005
Congenital anomaly of skeletal bone 8447006
Congenital anomaly of digestive organ 128332003
Congenital anomaly of musculoskeletal system 73573004
Genodermatosis 239001006
Congenital abnormality of oral cavity 282041002
Malformation of tooth 422775003
Congenital anomaly of jaw 95473006
Disorder of bone development 371521007
Disorder of hair 279425004
Congenital ectodermal defect 254154003
Congenital anomaly of skin 199879009
Disorder of tooth development 371136004
Disorder of skin appendage 238714008
Congenital anomaly of mouth 128334002
Disorder of bone 76069003
Hair finding 247522004
Disorder of embryonic structure 609521009
Congenital anomaly of integument 38164009
Tooth disorder 234947003
Disorder of skeletal system 88230002
Disorder of skin 95320005
Congenital anomaly of head 87290003
Bone finding 118953000
Congenital malformation of upper alimentary tract 275262008
Disorder of teeth AND/OR supporting structures 105995000
Disorder of digestive organ 76712006
Disorder of musculoskeletal system 928000
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 integument 128598002
Oral cavity finding 116337000
Disorder of jaw 37156001
Musculoskeletal finding 106028002
Disease of mouth 118938008
Skin AND/OR mucosa finding 415531008
Disorder of soft tissue 19660004
Congenital malformation 276654001
Integumentary system finding 106077005
Finding of mouth region 423066003
Disorder of head 118934005
General finding of soft tissue 248402002
Disorder of upper digestive tract 50410009
Developmental disorder 5294002
Finding of head region 298364001
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

cpt crosswalks

Rules-based maps relating CPT® codes to and from SNOMED CT® clinical concepts. Forward and backward mapping allows for easy transition between code sets. Map-A-Code crosswalk tool easily crosswalks multiple codes between the code sets.

Access to this feature is available in the following products:

CPT® to SNOMED Crosswalks

Thank you for choosing Find-A-Code, please Sign In to remove ads.

MY NEWSLETTERS

FEES

FACILITY

RISK ADJUSTMENT

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

Cranioectodermal dysplasia 254093009

SNOMED CT code