Xeroderma pigmentosum and Cockayne syndrome complex 719819004

SNOMED CT code

SNOMED code

719819004

name

Xeroderma pigmentosum and Cockayne syndrome complex

status

active

date introduced

2017-01-31

fully specified name(s)

Xeroderma pigmentosum and Cockayne syndrome complex (disorder)

synonyms

Xeroderma pigmentosum and Cockayne syndrome complex

attributes - group2

Associated morphology

Pigment deposition 51083003

Finding site

Skin structure 39937001

Pathological process

Pathological developmental process 308490002

attributes - group1

Occurrence

Congenital 255399007

Finding site

Central nervous system tract structure 57592002

Pathological process

Pathological developmental process 308490002

Associated morphology

Morphologically abnormal structure 49755003

attributes - group3

Interprets

Moistness of skin 364532007

Has interpretation

Decreased 1250004

parents

Cockayne syndrome 21086008
Xeroderma pigmentosum 44600005

hierarchies

a selection of possible paths

SNOMED CT Concept 138875005
Clinical finding 404684003
Central nervous system finding 246556002
Disorder of the central nervous system 23853001
Congenital anomaly of central nervous system 128124001
Cockayne syndrome 21086008
Xeroderma pigmentosum and Cockayne syndrome complex 719819004

SNOMED CT Concept 138875005
Clinical finding 404684003
Integumentary system finding 106077005
Disorder of integument 128598002
Hereditary disorder of the integument 363185004
Xeroderma pigmentosum 44600005
Xeroderma pigmentosum and Cockayne syndrome complex 719819004

ancestors

sorted most to least specific

Cockayne syndrome 21086008
Xeroderma pigmentosum 44600005
Multiple malformation syndrome with senile-like appearance 12674005
Developmental hereditary disorder 363070008
Congenital anomaly of central nervous system 128124001
Hereditary disorder of nervous system 363235000
Hereditary cancer-predisposing syndrome 699346009
Hereditary disorder of the integument 363185004
Skin deposits 40449001
Xeroderma 52475004
Genetic disorder of skin pigmentation 724839001
Autosomal recessive hereditary disorder 85995004
Multiple system malformation syndrome 82354003
Disorder of the central nervous system 23853001
Degenerative skin disorder 396325007
Finding of moistness of skin 297949006
Disorder of skin pigmentation 46690002
Autosomal hereditary disorder 1899006
Congenital anomaly of nervous system 88425004
Hereditary disorder by system 363137000
Congenital malformation syndrome 400038003
Hereditary disease 32895009
Disorder of nervous system 118940003
Degenerative disorder 362975008
Disorder of pigmentation 414032001
Central nervous system finding 246556002
Skin lesion 95324001
Congenital malformation 276654001
Genetic disease 782964007
Disorder of skin 95320005
Soft tissue lesion 239953001
Lesion of skin and/or skin-associated mucous membrane 714974000
Developmental disorder 5294002
Congenital disease 66091009
Skin finding 106076001
Disorder of skin and/or subcutaneous tissue 80659006
Skin or mucosa lesion 247440002
Disorder of integument 128598002
Skin AND/OR mucosa finding 415531008
Disorder of soft tissue 19660004
Disorder of body system 362965005
Integumentary system finding 106077005
General finding of soft tissue 248402002
Disease 64572001
Clinical finding 404684003
SNOMED CT Concept 138875005

cpt crosswalks

Rules-based maps relating CPT® codes to and from SNOMED CT® clinical concepts. Forward and backward mapping allows for easy transition between code sets. Map-A-Code crosswalk tool easily crosswalks multiple codes between the code sets.

Access to this feature is available in the following products:

CPT® to SNOMED Crosswalks

Thank you for choosing Find-A-Code, please Sign In to remove ads.

MY NEWSLETTERS

FEES

FACILITY

RISK ADJUSTMENT

SNOMED CT Concept 138875005

Clinical finding 404684003

Central nervous system finding 246556002

Disorder of the central nervous system 23853001

Congenital anomaly of central nervous system 128124001

Cockayne syndrome 21086008

Xeroderma pigmentosum and Cockayne syndrome complex 719819004

SNOMED CT code