Epidermolysis bullosa simplex with hypodontia 254177003

SNOMED CT code

SNOMED code

254177003

name

Epidermolysis bullosa simplex with hypodontia

status

active

date introduced

2002-01-31

fully specified name(s)

Epidermolysis bullosa simplex with hypodontia (disorder)

synonyms

Epidermolysis bullosa simplex with hypodontia
Kallin's syndrome

attributes - group1

Pathological process

Pathological developmental process 308490002

Occurrence

Congenital 255399007

Associated morphology

Epidermolysis 85269007

Finding site

Skin structure 39937001

attributes - group2

Associated morphology

Congenital abnormal number 61295008

Occurrence

Congenital 255399007

Pathological process

Pathological developmental process 308490002

Finding site

Tooth structure 38199008

attributes - group3

Pathological process

Pathological developmental process 308490002

Associated morphology

Absence 418560003

Finding site

Tooth structure 38199008

Occurrence

Congenital 255399007

parents

Developmental absence of tooth 234951001
Partial congenital absence of teeth 64969001
Epidermolysis bullosa simplex 67144006
Congenital absence of jaw 91922000
Congenital absence of mouth 91946007

hierarchies

a selection of possible paths

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Developmental disorder 5294002
Developmental hereditary disorder 363070008
Developmental absence of tooth 234951001
Epidermolysis bullosa simplex with hypodontia 254177003

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
Congenital anomaly in number of teeth 410066003
Partial congenital absence of teeth 64969001
Epidermolysis bullosa simplex with hypodontia 254177003

SNOMED CT Concept 138875005
Clinical finding 404684003
Integumentary system finding 106077005
Disorder of integument 128598002
Hereditary disorder of the integument 363185004
Epidermolysis bullosa 61003004
Epidermolysis bullosa simplex 67144006
Epidermolysis bullosa simplex with hypodontia 254177003

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Disorder of head 118934005
Disorder of jaw 37156001
Congenital anomaly of jaw 95473006
Congenital absence of jaw 91922000
Epidermolysis bullosa simplex with hypodontia 254177003

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Disorder of head 118934005
Disease of mouth 118938008
Congenital anomaly of mouth 128334002
Congenital absence of mouth 91946007
Epidermolysis bullosa simplex with hypodontia 254177003

ancestors

sorted most to least specific

Developmental absence of tooth 234951001
Partial congenital absence of teeth 64969001
Epidermolysis bullosa simplex 67144006
Congenital absence of jaw 91922000
Congenital absence of mouth 91946007
Hereditary disorder of tooth 1148766007
Congenital anomaly in number of teeth 410066003
Epidermolysis bullosa 61003004
Congenital partial absence of alimentary tract 83028006
Congenital anomaly of tooth 422977003
Genodermatosis 239001006
Developmental hereditary disorder 363070008
Digestive system hereditary disorder 363080007
Hereditary disorder of the integument 363185004
Degenerative skin disorder 396325007
Congenital absence of alimentary tract 66793004
Congenital anomaly of digestive organ 128332003
Congenital anomaly of skin 199879009
Congenital anomaly of jaw 95473006
Malformation of tooth 422775003
Hereditary disorder by system 363137000
Congenital abnormality of oral cavity 282041002
Degenerative disorder 362975008
Congenital anomaly of integument 38164009
Congenital anomaly of mouth 128334002
Hereditary disease 32895009
Disorder of tooth development 371136004
Disorder of skin 95320005
Tooth disorder 234947003
Genetic disease 782964007
Skin finding 106076001
Congenital anomaly of head 87290003
Congenital malformation of upper alimentary tract 275262008
Disorder of skin and/or subcutaneous tissue 80659006
Disorder of teeth AND/OR supporting structures 105995000
Disorder of integument 128598002
Tooth finding 278544002
Disorder of digestive organ 76712006
Congenital anomaly of digestive tract 95470009
Skin AND/OR mucosa finding 415531008
Disorder of soft tissue 19660004
Oral cavity finding 116337000
Congenital anomaly of digestive system 69518005
Integumentary system finding 106077005
Disorder of jaw 37156001
Disease of mouth 118938008
General finding of soft tissue 248402002
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

Disease 64572001

Developmental disorder 5294002

Developmental hereditary disorder 363070008

Developmental absence of tooth 234951001

Epidermolysis bullosa simplex with hypodontia 254177003

SNOMED CT code