Oculoosteocutaneous syndrome 722061006

SNOMED CT code

SNOMED code

722061006

name

Oculoosteocutaneous syndrome

status

active

date introduced

2017-01-31

fully specified name(s)

Oculoosteocutaneous syndrome (disorder)

synonyms

Oculoosteocutaneous syndrome

attributes - group2

Pathological process

Pathological developmental process 308490002

Associated morphology

Morphologically abnormal structure 49755003

Finding site

Hair structure 386045008

Occurrence

Congenital 255399007

attributes - group1

Occurrence

Congenital 255399007

Pathological process

Pathological developmental process 308490002

Finding site

Ectoderm structure 63206006

Associated morphology

Dysplasia 25723000

attributes - group3

Associated morphology

Morphologically abnormal structure 49755003

Pathological process

Pathological developmental process 308490002

Finding site

Tooth structure 38199008

Occurrence

Congenital 255399007

parents

Hereditary disorder of tooth 1148766007
Ectodermal dysplasia with hair-tooth defects 239027006
Developmental hereditary disorder 363070008
Hereditary disorder of the integument 363185004
Autosomal recessive hereditary disorder 85995004

hierarchies

a selection of possible paths

SNOMED CT Concept 138875005
Clinical finding 404684003
Digestive system finding 386617003
Disorder of digestive system 53619000
Digestive system hereditary disorder 363080007
Hereditary disorder of tooth 1148766007
Oculoosteocutaneous syndrome 722061006

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
Oculoosteocutaneous syndrome 722061006

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Developmental disorder 5294002
Developmental hereditary disorder 363070008
Oculoosteocutaneous syndrome 722061006

SNOMED CT Concept 138875005
Clinical finding 404684003
Integumentary system finding 106077005
Disorder of integument 128598002
Hereditary disorder of the integument 363185004
Oculoosteocutaneous syndrome 722061006

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Genetic disease 782964007
Hereditary disease 32895009
Autosomal hereditary disorder 1899006
Autosomal recessive hereditary disorder 85995004
Oculoosteocutaneous syndrome 722061006

ancestors

sorted most to least specific

Hereditary disorder of tooth 1148766007
Ectodermal dysplasia with hair-tooth defects 239027006
Developmental hereditary disorder 363070008
Hereditary disorder of the integument 363185004
Autosomal recessive hereditary disorder 85995004
Congenital anomaly of tooth 422977003
Autosomal hereditary disorder 1899006
Digestive system hereditary disorder 363080007
Congenital anomaly of hair 65033000
Ectodermal dysplasia 8654005
Congenital anomaly of digestive organ 128332003
Hereditary disorder by system 363137000
Genodermatosis 239001006
Congenital abnormality of oral cavity 282041002
Malformation of tooth 422775003
Congenital anomaly of jaw 95473006
Disorder of hair 279425004
Congenital ectodermal defect 254154003
Hereditary disease 32895009
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
Tooth disorder 234947003
Genetic disease 782964007
Congenital anomaly of integument 38164009
Disorder of skin 95320005
Congenital anomaly of head 87290003
Congenital malformation of upper alimentary tract 275262008
Disorder of teeth AND/OR supporting structures 105995000
Tooth finding 278544002
Disorder of digestive organ 76712006
Skin finding 106076001
Disorder of skin and/or subcutaneous tissue 80659006
Congenital anomaly of digestive tract 95470009
Oral cavity finding 116337000
Congenital anomaly of digestive system 69518005
Disorder of integument 128598002
Disease of mouth 118938008
Disorder of jaw 37156001
Skin AND/OR mucosa finding 415531008
Disorder of soft tissue 19660004
Finding of mouth region 423066003
Congenital malformation 276654001
Integumentary system finding 106077005
Disorder of head 118934005
Disorder of upper digestive tract 50410009
General finding of soft tissue 248402002
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

Digestive system finding 386617003

Disorder of digestive system 53619000

Digestive system hereditary disorder 363080007

Hereditary disorder of tooth 1148766007

Oculoosteocutaneous syndrome 722061006

SNOMED CT code