Verloes Bourguignon syndrome 716195006

SNOMED CT code

SNOMED code

716195006

name

Verloes Bourguignon syndrome

status

active

date introduced

2016-07-31

fully specified name(s)

Autosomal recessive brachyolmia and amelogenesis imperfecta syndrome (disorder)

synonyms

Autosomal recessive brachyolmia and amelogenesis imperfecta syndrome
Platyspondyly amelogenesis imperfecta
Verloes Bourguignon syndrome
Brachyolmia and amelogenesis imperfecta syndrome

attributes - group1

Occurrence

Congenital 255399007

Pathological process

Pathological developmental process 308490002

Finding site

Bone structure 272673000

Associated morphology

Dysplasia 25723000

attributes - group4

Pathological process

Pathological developmental process 308490002

Finding site

Enamel structure 76993005

Associated morphology

Morphologically abnormal structure 49755003

Occurrence

Congenital 255399007

attributes - group3

Interprets

Height / growth measure 271603002

parents

Brachyolmia 254088006
Amelogenesis imperfecta 78494001
Autosomal recessive hereditary disorder 85995004

hierarchies

a selection of possible paths

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Developmental disorder 5294002
Developmental hereditary disorder 363070008
Brachyolmia 254088006
Verloes Bourguignon syndrome 716195006

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Developmental disorder 5294002
Developmental hereditary disorder 363070008
Amelogenesis imperfecta 78494001
Verloes Bourguignon syndrome 716195006

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Genetic disease 782964007
Hereditary disease 32895009
Autosomal hereditary disorder 1899006
Autosomal recessive hereditary disorder 85995004
Verloes Bourguignon syndrome 716195006

ancestors

sorted most to least specific

Brachyolmia 254088006
Amelogenesis imperfecta 78494001
Autosomal recessive hereditary disorder 85995004
Autosomal hereditary disorder 1899006
Hereditary disorder of tooth 1148766007
Congenital malformation syndromes associated with short stature 205808005
Spondylodysplastic group 278708009
Developmental hereditary disorder 363070008
Hereditary disorder of musculoskeletal system 363212003
Congenital anomaly of tooth 422977003
Disorder of hard tissues of teeth 46557008
Short stature disorder 237836003
Skeletal dysplasia 105986008
Congenital anomaly of digestive organ 128332003
Digestive system hereditary disorder 363080007
Congenital malformation syndrome 400038003
Congenital anomaly of skeletal bone 8447006
Congenital abnormality of oral cavity 282041002
Malformation of tooth 422775003
Congenital anomaly of jaw 95473006
Disorder of stature 237834000
Congenital anomaly of musculoskeletal system 73573004
Hereditary disorder by system 363137000
Disorder of bone development 371521007
Disorder of tooth development 371136004
Congenital anomaly of mouth 128334002
Hereditary disease 32895009
Tooth disorder 234947003
General finding of height 248327008
Finding of general physiological development 271616002
Disorder of bone 76069003
Congenital anomaly of head 87290003
Congenital malformation of upper alimentary tract 275262008
Genetic disease 782964007
Disorder of teeth AND/OR supporting structures 105995000
Height / growth finding 365714001
Tooth finding 278544002
Disorder of digestive organ 76712006
Disorder of skeletal system 88230002
Bone finding 118953000
Congenital anomaly of digestive tract 95470009
Oral cavity finding 116337000
Body measurement finding 365605003
Congenital anomaly of digestive system 69518005
Disease of mouth 118938008
Disorder of jaw 37156001
Disorder of musculoskeletal system 928000
Finding of mouth region 423066003
Congenital malformation 276654001
Disorder of head 118934005
Musculoskeletal finding 106028002
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

Brachyolmia 254088006

Verloes Bourguignon syndrome 716195006

SNOMED CT code