Harlequin ichthyosis 205548006

SNOMED CT code

SNOMED code

205548006

name

Harlequin ichthyosis

status

active

date introduced

2002-01-31

fully specified name(s)

Harlequin ichthyosis (disorder)

synonyms

Harlequin ichthyosis

attributes - group1

Pathological process

Pathological developmental process 308490002

Associated morphology

Hyperkeratosis 26996000

Finding site

Entire skin 181469002

Occurrence

Congenital 255399007

attributes - group3

Associated morphology

Eversion 4196002

Pathological process

Pathological developmental process 308490002

Occurrence

Congenital 255399007

Finding site

Eyelid structure 80243003

attributes - group2

Associated morphology

Eversion 4196002

Pathological process

Pathological developmental process 308490002

Finding site

Lip structure 48477009

Occurrence

Congenital 255399007

attributes - group4

Has interpretation

Abnormal 263654008

Interprets

Keratinization 44138005

parents

Congenital ectropion of lip 204647002
Congenital ectropion 26590002
Digestive system hereditary disorder 363080007
Hereditary disorder of the visual system 363343008
Autosomal recessive ichthyosis 402772005

hierarchies

a selection of possible paths

SNOMED CT Concept 138875005
Clinical finding 404684003
General finding of soft tissue 248402002
Disorder of soft tissue 19660004
Congenital deformity of soft tissue 673791000119108
Congenital ectropion of lip 204647002
Harlequin ichthyosis 205548006

SNOMED CT Concept 138875005
Clinical finding 404684003
Deformity 417893002
Deformity of eyelid 430960001
Ectropion 62909004
Congenital ectropion 26590002
Harlequin ichthyosis 205548006

SNOMED CT Concept 138875005
Clinical finding 404684003
Digestive system finding 386617003
Disorder of digestive system 53619000
Digestive system hereditary disorder 363080007
Harlequin ichthyosis 205548006

SNOMED CT Concept 138875005
Clinical finding 404684003
Eye / vision finding 118235002
Visual system disorder 128127008
Hereditary disorder of the visual system 363343008
Harlequin ichthyosis 205548006

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
Harlequin ichthyosis 205548006

ancestors

sorted most to least specific

Congenital ectropion of lip 204647002
Congenital ectropion 26590002
Digestive system hereditary disorder 363080007
Hereditary disorder of the visual system 363343008
Autosomal recessive ichthyosis 402772005
Congenital anomaly of lip 109549008
Congenital deformity of face 398206004
Congenital ichthyosis of skin 13059002
Congenital deformity of soft tissue 673791000119108
Ectropion 62909004
Congenital anomaly of eyelid 91158006
Autosomal recessive hereditary disorder 85995004
Congenital anomaly of mouth 128334002
Congenital deformity 276655000
Genodermatosis 239001006
Congenital anomaly of face 398302004
Disorder of lip 90678009
Deformity of eyelid 430960001
Congenital anomaly of ocular adnexa 128327004
Autosomal hereditary disorder 1899006
Inherited disorder of keratinization 254214009
Developmental hereditary disorder 363070008
Ichthyosis 782957005
Rough skin 816995008
Deformity of tissue 416499003
Congenital anomaly of skin 199879009
Congenital malformation of upper alimentary tract 275262008
Congenital anomaly of head 87290003
Deformity 417893002
Disorder of keratinization 277905003
Keratoderma 707209001
Lip finding 248174008
Disorder of oral soft tissues 41188003
Disorder of eyelid 60113004
Congenital anomaly of visual system 127329003
Hereditary disorder of the integument 363185004
Disease of mouth 118938008
Hereditary disorder by system 363137000
Congenital anomaly of integument 38164009
Disorder of face 118930001
Disorder of ocular adnexa 118941004
Keratosis 254666005
Disorder of skin 95320005
Congenital anomaly of digestive tract 95470009
Abnormal keratinization 69707008
Disorder of soft tissue of head 280131007
Eyelid finding 246812007
Hereditary disease 32895009
Disorder of upper digestive tract 50410009
Finding of mouth region 423066003
Disorder of eye region 371409005
Skin finding 106076001
Finding of face 301310005
Congenital anomaly of digestive system 69518005
Disorder of skin and/or subcutaneous tissue 80659006
Functional finding 118228005
Disorder of head 118934005
Congenital malformation 276654001
Genetic disease 782964007
Visual system disorder 128127008
Disorder of integument 128598002
Disorder of soft tissue 19660004
Disorder of digestive tract 84410009
Finding of head region 298364001
Skin AND/OR mucosa finding 415531008
Head finding 406122000
Developmental disorder 5294002
Eye / vision finding 118235002
Integumentary system finding 106077005
General finding of soft tissue 248402002
Disorder of digestive system 53619000
Congenital disease 66091009
Finding of head and neck region 118254002
Disorder of body system 362965005
Digestive system finding 386617003
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

General finding of soft tissue 248402002

Disorder of soft tissue 19660004

Congenital deformity of soft tissue 673791000119108

Congenital ectropion of lip 204647002

Harlequin ichthyosis 205548006

SNOMED CT code