Keratosis linearis, ichthyosis congenita, sclerosing keratoderma syndrome 763775000

SNOMED CT code

SNOMED code

763775000

name

Keratosis linearis, ichthyosis congenita, sclerosing keratoderma syndrome

status

active

date introduced

2018-07-31

fully specified name(s)

Keratosis linearis, ichthyosis congenita, sclerosing keratoderma syndrome (disorder)

synonyms

KLICK syndrome
Keratosis linearis, ichthyosis congenita, sclerosing keratoderma syndrome

attributes - group1

Pathological process

Pathological developmental process 308490002

Finding site

Entire skin 181469002

Occurrence

Congenital 255399007

Associated morphology

Hyperkeratosis 26996000

attributes - group4

Associated morphology

Hyperkeratosis 26996000

Finding site

Entire skin of sole of foot 181566006

attributes - group2

Finding site

Entire skin of palmar area of hand 181544004

Associated morphology

Hyperkeratosis 26996000

attributes - group3

Has interpretation

Abnormal 263654008

Interprets

Keratinization 44138005

parents

Hereditary diffuse palmoplantar keratoderma 400123002
Autosomal recessive ichthyosis 402772005
Rough skin of hands 829993001

hierarchies

a selection of possible paths

SNOMED CT Concept 138875005
Clinical finding 404684003
Integumentary system finding 106077005
Disorder of integument 128598002
Hereditary disorder of the integument 363185004
Hereditary palmoplantar keratoderma 239066003
Hereditary diffuse palmoplantar keratoderma 400123002
Keratosis linearis, ichthyosis congenita, sclerosing keratoderma syndrome 763775000

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
Keratosis linearis, ichthyosis congenita, sclerosing keratoderma syndrome 763775000

SNOMED CT Concept 138875005
Clinical finding 404684003
Finding of limb structure 302293008
Finding of upper limb 116307009
Finding of hand region 116311003
Rough skin of hands 829993001
Keratosis linearis, ichthyosis congenita, sclerosing keratoderma syndrome 763775000

ancestors

sorted most to least specific

Hereditary diffuse palmoplantar keratoderma 400123002
Autosomal recessive ichthyosis 402772005
Rough skin of hands 829993001
Hereditary palmoplantar keratoderma 239066003
Congenital ichthyosis of skin 13059002
Autosomal recessive hereditary disorder 85995004
Genodermatosis 239001006
Palmoplantar keratoderma 706885006
Autosomal hereditary disorder 1899006
Inherited disorder of keratinization 254214009
Developmental hereditary disorder 363070008
Ichthyosis 782957005
Rough skin 816995008
Hereditary disorder of the integument 363185004
Congenital anomaly of skin 199879009
Disorder of foot 118932009
Disorder of keratinization 277905003
Keratoderma 707209001
Disorder of hand 118933004
Disorder of skin of upper limb 400160003
Disorder of skin of lower limb 400202001
Congenital anomaly of integument 38164009
Finding of hand region 116311003
Finding of foot region 116316008
Hereditary disorder by system 363137000
Keratosis 254666005
Disorder of skin 95320005
Disorder of soft tissue of upper limb 280135003
Disorder of soft tissue of lower limb 280136002
Disorder of free lower limb 700012005
Abnormal keratinization 69707008
Finding of ankle or foot 419518009
Hereditary disease 32895009
Skin finding 106076001
Congenital malformation 276654001
Disorder of upper limb 118947000
Disorder of lower limb 118937003
Disorder of skin and/or subcutaneous tissue 80659006
Disorder of soft tissue of limb 280134004
Functional finding 118228005
Disorder of integument 128598002
Finding of upper limb 116307009
Finding of lower limb 116312005
Genetic disease 782964007
Developmental disorder 5294002
Skin AND/OR mucosa finding 415531008
Congenital disease 66091009
Disorder of limb 128605003
Disorder of soft tissue 19660004
Integumentary system finding 106077005
Finding of limb structure 302293008
Disorder of body system 362965005
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

Integumentary system finding 106077005

Disorder of integument 128598002

Hereditary disorder of the integument 363185004

Hereditary palmoplantar keratoderma 239066003

Hereditary diffuse palmoplantar keratoderma 400123002

Keratosis linearis, ichthyosis congenita, sclerosing keratoderma syndrome 763775000

SNOMED CT code