Hereditary skin peeling syndrome 724838009

SNOMED CT code

SNOMED code

724838009

name

Hereditary skin peeling syndrome

status

active

date introduced

2017-07-31

fully specified name(s)

Hereditary skin peeling syndrome (disorder)

synonyms

Hereditary skin peeling syndrome
Peeling skin syndrome
Familial continuous skin peeling syndrome

attributes - group1

Occurrence

Congenital 255399007

Finding site

Entire skin 181469002

Associated morphology

Hyperkeratosis 26996000

Pathological process

Pathological developmental process 308490002

attributes - group4

Associated morphology

Exfoliative lesion 400183000

Finding site

Skin structure 39937001

attributes - group3

Has interpretation

Abnormal 263654008

Interprets

Keratinization 44138005

parents

Skin peeling disorder 238643009
Autosomal recessive ichthyosis 402772005

children

Acral peeling skin syndrome 709416009
Generalized peeling skin syndrome 718749004

hierarchies

a selection of possible paths

SNOMED CT Concept 138875005
Clinical finding 404684003
Integumentary system finding 106077005
Disorder of integument 128598002
Disorder of keratinization 277905003
Skin peeling disorder 238643009
Hereditary skin peeling syndrome 724838009

SNOMED CT Concept 138875005
Clinical finding 404684003
Integumentary system finding 106077005
Skin finding 106076001
Rough skin 816995008
Congenital ichthyosis of skin 13059002
Autosomal recessive ichthyosis 402772005
Hereditary skin peeling syndrome 724838009

ancestors

sorted most to least specific

Skin peeling disorder 238643009
Autosomal recessive ichthyosis 402772005
Congenital ichthyosis of skin 13059002
Skin lesion 95324001
Autosomal recessive hereditary disorder 85995004
Genodermatosis 239001006
Soft tissue lesion 239953001
Autosomal hereditary disorder 1899006
Inherited disorder of keratinization 254214009
Developmental hereditary disorder 363070008
Ichthyosis 782957005
Rough skin 816995008
Lesion of skin and/or skin-associated mucous membrane 714974000
Disorder of keratinization 277905003
Congenital anomaly of skin 199879009
Keratoderma 707209001
Skin or mucosa lesion 247440002
Hereditary disorder of the integument 363185004
Congenital anomaly of integument 38164009
Abnormal keratinization 69707008
Keratosis 254666005
Disorder of skin 95320005
Hereditary disorder by system 363137000
Hereditary disease 32895009
Skin finding 106076001
Congenital malformation 276654001
Functional finding 118228005
Disorder of skin and/or subcutaneous tissue 80659006
Disorder of integument 128598002
Disorder of soft tissue 19660004
Genetic disease 782964007
Developmental disorder 5294002
Skin AND/OR mucosa finding 415531008
Congenital disease 66091009
Integumentary system finding 106077005
General finding of soft tissue 248402002
Disorder of body system 362965005
Disease 64572001
Clinical finding 404684003
SNOMED CT Concept 138875005

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SNOMED CT Concept 138875005

Clinical finding 404684003

Integumentary system finding 106077005

Disorder of integument 128598002

Disorder of keratinization 277905003

Skin peeling disorder 238643009

Hereditary skin peeling syndrome 724838009

SNOMED CT code