Trichodysplasia with amelogenesis imperfecta syndrome 719911000

SNOMED CT code

SNOMED code

719911000

name

Trichodysplasia with amelogenesis imperfecta syndrome

status

active

date introduced

2017-01-31

fully specified name(s)

Trichodysplasia with amelogenesis imperfecta syndrome (disorder)

synonyms

Trichodysplasia with amelogenesis imperfecta syndrome

attributes - group2

Pathological process

Pathological developmental process 308490002

Associated morphology

Morphologically abnormal structure 49755003

Occurrence

Congenital 255399007

Finding site

Enamel structure 76993005

attributes - group3

Pathological process

Pathological developmental process 308490002

Associated morphology

Morphologically abnormal structure 49755003

Occurrence

Congenital 255399007

Finding site

Skin structure 39937001

attributes - group1

Finding site

Ectoderm structure 63206006

Occurrence

Congenital 255399007

Pathological process

Pathological developmental process 308490002

Associated morphology

Dysplasia 25723000

parents

X-linked recessive hereditary disease 1162976004
Hereditary disorder of the integument 363185004
Amelogenesis imperfecta 78494001
Ectodermal dysplasia 8654005

hierarchies

a selection of possible paths

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Genetic disease 782964007
Hereditary disease 32895009
Sex-linked hereditary disorder 82852009
X-linked hereditary disease 128430005
X-linked recessive hereditary disease 1162976004
Trichodysplasia with amelogenesis imperfecta syndrome 719911000

SNOMED CT Concept 138875005
Clinical finding 404684003
Integumentary system finding 106077005
Disorder of integument 128598002
Hereditary disorder of the integument 363185004
Trichodysplasia with amelogenesis imperfecta syndrome 719911000

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Developmental disorder 5294002
Developmental hereditary disorder 363070008
Amelogenesis imperfecta 78494001
Trichodysplasia with amelogenesis imperfecta syndrome 719911000

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Disorder of embryonic structure 609521009
Congenital ectodermal defect 254154003
Ectodermal dysplasia 8654005
Trichodysplasia with amelogenesis imperfecta syndrome 719911000

ancestors

sorted most to least specific

X-linked recessive hereditary disease 1162976004
Hereditary disorder of the integument 363185004
Amelogenesis imperfecta 78494001
Ectodermal dysplasia 8654005
X-linked hereditary disease 128430005
Hereditary disorder of tooth 1148766007
Genodermatosis 239001006
Developmental hereditary disorder 363070008
Congenital anomaly of tooth 422977003
Disorder of hard tissues of teeth 46557008
Congenital ectodermal defect 254154003
Sex-linked hereditary disorder 82852009
Congenital anomaly of skin 199879009
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
Disorder of embryonic structure 609521009
Congenital anomaly of integument 38164009
Hereditary disorder by system 363137000
Disorder of skin 95320005
Disorder of tooth development 371136004
Congenital anomaly of mouth 128334002
Hereditary disease 32895009
Tooth disorder 234947003
Skin finding 106076001
Disorder of skin and/or subcutaneous tissue 80659006
Congenital anomaly of head 87290003
Congenital malformation of upper alimentary tract 275262008
Genetic disease 782964007
Disorder of integument 128598002
Disorder of teeth AND/OR supporting structures 105995000
Tooth finding 278544002
Disorder of digestive organ 76712006
Skin AND/OR mucosa finding 415531008
Disorder of soft tissue 19660004
Congenital anomaly of digestive tract 95470009
Integumentary system finding 106077005
Oral cavity finding 116337000
Congenital anomaly of digestive system 69518005
Disease of mouth 118938008
Disorder of jaw 37156001
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

Genetic disease 782964007

Hereditary disease 32895009

Sex-linked hereditary disorder 82852009

X-linked hereditary disease 128430005

X-linked recessive hereditary disease 1162976004

Trichodysplasia with amelogenesis imperfecta syndrome 719911000

SNOMED CT code