Polyvalvular heart disease syndrome 723448007

SNOMED CT code

SNOMED code

723448007

name

Polyvalvular heart disease syndrome

status

active

date introduced

2017-07-31

fully specified name(s)

Polyvalvular heart disease syndrome (disorder)

synonyms

Polyvalvular heart disease syndrome

attributes - group1

Occurrence

Congenital 255399007

Finding site

Face structure 89545001

Pathological process

Pathological developmental process 308490002

Associated morphology

Morphologically abnormal structure 49755003

attributes - group2

Pathological process

Pathological developmental process 308490002

Associated morphology

Dysplasia 25723000

Occurrence

Congenital 255399007

Finding site

Cardiac valve structure 17401000

parents

Autosomal dominant hereditary disorder 11164009
Cardiovascular system hereditary disorder 363005004
Developmental hereditary disorder 363070008
Multiple malformation syndrome with facial defects as major feature 65094009
Congenital dysplasia of cardiac valve 718128009

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
Polyvalvular heart disease syndrome 723448007

SNOMED CT Concept 138875005
Clinical finding 404684003
Cardiovascular finding 106063007
Disorder of cardiovascular system 49601007
Cardiovascular system hereditary disorder 363005004
Polyvalvular heart disease syndrome 723448007

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Developmental disorder 5294002
Developmental hereditary disorder 363070008
Polyvalvular heart disease syndrome 723448007

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Disorder of head 118934005
Disorder of face 118930001
Congenital anomaly of face 398302004
Multiple malformation syndrome with facial defects as major feature 65094009
Polyvalvular heart disease syndrome 723448007

SNOMED CT Concept 138875005
Clinical finding 404684003
Cardiovascular finding 106063007
Cardiac finding 301095005
Heart valve finding 301098007
Heart valve disorder 368009
Congenital anomaly of heart valve 70320004
Congenital dysplasia of cardiac valve 718128009
Polyvalvular heart disease syndrome 723448007

ancestors

sorted most to least specific

Autosomal dominant hereditary disorder 11164009
Cardiovascular system hereditary disorder 363005004
Developmental hereditary disorder 363070008
Multiple malformation syndrome with facial defects as major feature 65094009
Congenital dysplasia of cardiac valve 718128009
Autosomal hereditary disorder 1899006
Hereditary disorder by system 363137000
Congenital anomaly of face 398302004
Congenital anomaly of heart valve 70320004
Multiple system malformation syndrome 82354003
Hereditary disease 32895009
Disorder of face 118930001
Congenital heart disease 13213009
Congenital malformation syndrome 400038003
Congenital anomaly of head 87290003
Heart valve disorder 368009
Genetic disease 782964007
Disorder of head 118934005
Structural disorder of heart 128599005
Finding of face 301310005
Heart valve finding 301098007
Congenital anomaly of cardiovascular structure of trunk 363028003
Congenital anomaly of thorax 363035006
Heart disease 56265001
Finding of head region 298364001
Congenital anomaly of cardiovascular system 9904008
Congenital anomaly of upper trunk 363037003
Head finding 406122000
Cardiac finding 301095005
Congenital anomaly of trunk 78626001
Disorder of mediastinum 49483002
Congenital cardiovascular disorder 762228008
Finding of head and neck region 118254002
Disorder of cardiovascular system 49601007
Congenital malformation 276654001
Disorder of thorax 118946009
Mediastinal finding 301296002
Viscus structure finding 406123005
Cardiovascular finding 106063007
Disorder of body system 362965005
Developmental disorder 5294002
Finding of region of thorax 298705000
Congenital disease 66091009
Disorder of thoracic segment of trunk 609622007
Disorder of trunk 128121009
Finding of upper trunk 609623002
Disease 64572001
Finding of trunk structure 302292003
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

Polyvalvular heart disease syndrome 723448007

SNOMED CT code