Thoracolaryngopelvic dysplasia 723556008

SNOMED CT code

SNOMED code

723556008

name

Thoracolaryngopelvic dysplasia

status

active

date introduced

2017-07-31

fully specified name(s)

Thoracolaryngopelvic dysplasia syndrome (disorder)

synonyms

Thoracolaryngopelvic dysplasia
Barnes syndrome
Thoracolaryngopelvic dysplasia syndrome

attributes - group2

Pathological process

Pathological developmental process 308490002

Occurrence

Congenital 255399007

Finding site

Bone structure of rib 113197003

Associated morphology

Dysplasia 25723000

attributes - group1

Pathological process

Pathological developmental process 308490002

Occurrence

Congenital 255399007

Finding site

Bone structure of pelvis 118645006

Associated morphology

Morphologically abnormal structure 49755003

parents

Autosomal dominant hereditary disorder 11164009
Short rib dysplasia 254050009
Developmental hereditary disorder 363070008
Hereditary disorder of musculoskeletal system 363212003
Congenital anomaly of pelvic bones 93017005

hierarchies

a selection of possible paths

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Genetic disease 782964007
Hereditary disease 32895009
Autosomal hereditary disorder 1899006
Autosomal dominant hereditary disorder 11164009
Thoracolaryngopelvic dysplasia 723556008

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Genetic disease 782964007
Short rib dysplasia 254050009
Thoracolaryngopelvic dysplasia 723556008

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Developmental disorder 5294002
Developmental hereditary disorder 363070008
Thoracolaryngopelvic dysplasia 723556008

SNOMED CT Concept 138875005
Clinical finding 404684003
Musculoskeletal finding 106028002
Disorder of musculoskeletal system 928000
Hereditary disorder of musculoskeletal system 363212003
Thoracolaryngopelvic dysplasia 723556008

SNOMED CT Concept 138875005
Clinical finding 404684003
Musculoskeletal finding 106028002
Bone finding 118953000
Finding of bone of pelvis 417470001
Congenital anomaly of pelvic bones 93017005
Thoracolaryngopelvic dysplasia 723556008

ancestors

sorted most to least specific

Autosomal dominant hereditary disorder 11164009
Short rib dysplasia 254050009
Developmental hereditary disorder 363070008
Hereditary disorder of musculoskeletal system 363212003
Congenital anomaly of pelvic bones 93017005
Autosomal hereditary disorder 1899006
Skeletal dysplasia 105986008
Hereditary disorder by system 363137000
Congenital anomaly of rib 123572006
Finding of bone of pelvis 417470001
Congenital anomaly of the pelvis 47583008
Hereditary disease 32895009
Congenital anomaly of body wall 363027008
Congenital anomaly of lower trunk 363030001
Congenital anomaly of skeletal bone 8447006
Congenital anomaly of thoracic cage 8649001
Disorder of pelvis 609620004
Genetic disease 782964007
Congenital anomaly of musculoskeletal structure of trunk 363032009
Congenital abnormality of lower limb and pelvic girdle 253937004
Disorder of bone development 371521007
Disorder of body wall 399986003
Finding of pelvis 609626005
Disorder of pelvic region of trunk 609619005
Congenital anomaly of thorax 363035006
Congenital anomaly of musculoskeletal system 73573004
Finding of pelvic region of trunk 609625009
Disorder of abdominopelvic segment of trunk 822988000
Disorder of bone 76069003
Disorder of thorax 118946009
Congenital anomaly of upper trunk 363037003
Disorder of skeletal system 88230002
Bone finding 118953000
Congenital anomaly of trunk 78626001
Finding of abdominopelvic segment of trunk 822987005
Finding of region of thorax 298705000
Disorder of thoracic segment of trunk 609622007
Congenital malformation 276654001
Disorder of musculoskeletal system 928000
Disorder of trunk 128121009
Finding of upper trunk 609623002
Developmental disorder 5294002
Musculoskeletal finding 106028002
Congenital disease 66091009
Disorder of body system 362965005
Finding of trunk structure 302292003
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

Autosomal hereditary disorder 1899006

Autosomal dominant hereditary disorder 11164009

Thoracolaryngopelvic dysplasia 723556008

SNOMED CT code