Marden Walker syndrome 449824004

SNOMED CT code

SNOMED code

449824004

name

Marden Walker syndrome

status

active

date introduced

2012-01-31

fully specified name(s)

Marden Walker syndrome (disorder)

synonyms

Marden Walker syndrome

attributes - group3

Interprets

Range of joint movement 364564000

Has interpretation

Decreased 1250004

attributes - group1

Occurrence

Congenital 255399007

Finding site

Face structure 89545001

Associated morphology

Morphologically abnormal structure 49755003

Pathological process

Pathological developmental process 308490002

attributes - group2

Occurrence

Congenital 255399007

Finding site

Structure of joint region 785818007

Associated morphology

Contracture 57048009

Pathological process

Pathological developmental process 308490002

parents

Arthrogryposis multiplex congenita 205402004
Inherited arthrogryposis 28204005
Multiple malformation syndrome with facial defects as major feature 65094009
Autosomal recessive hereditary disorder 85995004

hierarchies

a selection of possible paths

SNOMED CT Concept 138875005
Clinical finding 404684003
Deformity 417893002
Congenital deformity 276655000
Arthrogryposis 111246005
Arthrogryposis multiplex congenita 205402004
Marden Walker syndrome 449824004

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Developmental disorder 5294002
Developmental hereditary disorder 363070008
Inherited arthrogryposis 28204005
Marden Walker syndrome 449824004

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
Marden Walker syndrome 449824004

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Genetic disease 782964007
Hereditary disease 32895009
Autosomal hereditary disorder 1899006
Autosomal recessive hereditary disorder 85995004
Marden Walker syndrome 449824004

ancestors

sorted most to least specific

Arthrogryposis multiplex congenita 205402004
Inherited arthrogryposis 28204005
Multiple malformation syndrome with facial defects as major feature 65094009
Autosomal recessive hereditary disorder 85995004
Arthrogryposis 111246005
Congenital anomaly of face 398302004
Autosomal hereditary disorder 1899006
Developmental hereditary disorder 363070008
Multiple system malformation syndrome 82354003
Contracture of multiple joints 202264009
Disorder of face 118930001
Hereditary disease 32895009
Congenital deformity 276655000
Congenital malformation syndrome 400038003
Congenital anomaly of head 87290003
Contracture of joint 7890003
Disorder of head 118934005
Genetic disease 782964007
Congenital malformation 276654001
Finding of face 301310005
Deformity 417893002
Developmental disorder 5294002
Movement disorder 60342002
Limitation of joint movement 70733008
Disorder of joint region 785875003
Finding of head region 298364001
Congenital disease 66091009
Head finding 406122000
Disease 64572001
Finding of range of joint movement 298180004
Finding of head and neck region 118254002
Finding of joint movement 298179002
Finding of movement 298325004
Clinical finding 404684003
SNOMED CT Concept 138875005

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SNOMED CT Concept 138875005

Clinical finding 404684003

Deformity 417893002

Congenital deformity 276655000

Arthrogryposis 111246005

Arthrogryposis multiplex congenita 205402004

Marden Walker syndrome 449824004

SNOMED CT code