Autosomal dominant popliteal pterygium syndrome 718222000

SNOMED CT code

SNOMED code

718222000

name

Autosomal dominant popliteal pterygium syndrome

status

active

date introduced

2016-07-31

fully specified name(s)

Autosomal dominant popliteal pterygium syndrome (disorder)

synonyms

Autosomal dominant popliteal pterygium syndrome
Facio-genito-popliteal syndrome
Popliteal web syndrome

attributes - group1

Pathological process

Pathological developmental process 308490002

Associated morphology

Congenital webbing 76640006

Occurrence

Congenital 255399007

Finding site

Popliteal region structure 6902008

parents

Autosomal dominant hereditary disorder 11164009
Developmental hereditary disorder 363070008
Popliteal pterygium syndrome 66783006

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
Autosomal dominant popliteal pterygium syndrome 718222000

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Developmental disorder 5294002
Developmental hereditary disorder 363070008
Autosomal dominant popliteal pterygium syndrome 718222000

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Disorder of joint region 785875003
Disorder of knee 128136007
Popliteal pterygium syndrome 66783006
Autosomal dominant popliteal pterygium syndrome 718222000

ancestors

sorted most to least specific

Autosomal dominant hereditary disorder 11164009
Developmental hereditary disorder 363070008
Popliteal pterygium syndrome 66783006
Autosomal hereditary disorder 1899006
Disorder of knee 128136007
Multiple malformation syndrome with limb defect as major feature 41443008
Congenital anomaly of lower limb 84773003
Hereditary disease 32895009
Finding of knee region 116314006
Multiple system malformation syndrome 82354003
Disorder of free lower limb 700012005
Disorder of joint region 785875003
Congenital abnormality of lower limb and pelvic girdle 253937004
Congenital anomaly of limb 60475009
Genetic disease 782964007
Congenital malformation syndrome 400038003
Disorder of lower limb 118937003
Finding of lower limb 116312005
Congenital malformation 276654001
Disorder of limb 128605003
Finding of limb structure 302293008
Developmental disorder 5294002
Congenital disease 66091009
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

Autosomal dominant popliteal pterygium syndrome 718222000

SNOMED CT code