Rozin Hertz Goodman syndrome 715986009

SNOMED CT code

SNOMED code

715986009

name

Rozin Hertz Goodman syndrome

status

active

date introduced

2016-07-31

fully specified name(s)

Camptodactyly with joint contracture and facial skeletal defect syndrome (disorder)

synonyms

Camptodactyly with joint contracture and facial skeletal defect syndrome
Rozin Hertz Goodman syndrome
Rozin camptodactyly syndrome

attributes - group2

Pathological process

Pathological developmental process 308490002

Occurrence

Congenital 255399007

Associated morphology

Fixed flexion deformity 788600005

Finding site

Musculoskeletal structure of digit 310791006

attributes - group4

Pathological process

Pathological developmental process 308490002

Associated morphology

Morphologically abnormal structure 49755003

Occurrence

Congenital 255399007

Finding site

Face structure 89545001

attributes - group1

Occurrence

Congenital 255399007

Pathological process

Pathological developmental process 308490002

Finding site

Structure of joint region 785818007

Associated morphology

Flexion contracture 785817002

attributes - group3

Interprets

Range of joint movement 364564000

Has interpretation

Decreased 1250004

parents

Camptodactyly 29271008
Flexion contracture 385522000
Multiple malformation syndrome with facial defects as major feature 65094009

hierarchies

a selection of possible paths

SNOMED CT Concept 138875005
Clinical finding 404684003
Finding of limb structure 302293008
Deformity of limb 445144002
Camptodactyly 29271008
Rozin Hertz Goodman syndrome 715986009

SNOMED CT Concept 138875005
Clinical finding 404684003
Deformity 417893002
Contracture of joint 7890003
Flexion contracture 385522000
Rozin Hertz Goodman syndrome 715986009

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
Rozin Hertz Goodman syndrome 715986009

ancestors

sorted most to least specific

Camptodactyly 29271008
Flexion contracture 385522000
Multiple malformation syndrome with facial defects as major feature 65094009
Congenital deformity 276655000
Contracture of joint 7890003
Congenital anomaly of face 398302004
Deformity of limb 445144002
Congenital anomaly of musculoskeletal system 73573004
Congenital abnormal shape of digit 92907008
Multiple system malformation syndrome 82354003
Deformity 417893002
Disorder of face 118930001
Congenital anomaly of digit 403855001
Movement disorder 60342002
Limitation of joint movement 70733008
Disorder of joint region 785875003
Congenital malformation syndrome 400038003
Congenital anomaly of head 87290003
Disorder of musculoskeletal system 928000
Disorder of head 118934005
Disorder of digit 128597007
Finding of range of joint movement 298180004
Finding of face 301310005
Musculoskeletal finding 106028002
Congenital anomaly of limb 60475009
Disorder of body system 362965005
Congenital malformation 276654001
Disorder of limb 128605003
Finding of joint movement 298179002
Finding of head region 298364001
Developmental disorder 5294002
Head finding 406122000
Finding of limb structure 302293008
Congenital disease 66091009
Finding of movement 298325004
Disease 64572001
Finding of head and neck region 118254002
Clinical finding 404684003
SNOMED CT Concept 138875005

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SNOMED CT Concept 138875005

Clinical finding 404684003

Finding of limb structure 302293008

Deformity of limb 445144002

Camptodactyly 29271008

Rozin Hertz Goodman syndrome 715986009

SNOMED CT code