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Ectodermal dysplasia 8654005 SNOMED CT code SNOMED code 8654005 name Ectodermal dysplasia status active date introduced 2002-01-31 fully specified name(s) Ectodermal dysplasia (disorder) synonyms Ectodermal dysplasia attributes - group1 Occurrence Congenital 255399007 Finding site Ectoderm structure 63206006 Pathological process Pathological developmental process 308490002 Associated morphology Dysplasia 25723000 attributes - group2 Pathological process Pathological developmental process 308490002 Associated morphology Morphologically abnormal structure 49755003 Finding site Skin structure 39937001 Occurrence Congenital 255399007 parents children Ackerman syndrome 722280000 Alopecia, contracture, dwarfism, intellectual disability syndrome 720979002 Amelo-onycho-hypohidrotic syndrome 715404000 Autosomal recessive popliteal pterygium syndrome 722376008 Barber-Say syndrome 408537003 Blepharocheilodontic syndrome 717911008 Cerebellar ataxia and ectodermal dysplasia 715371006 Choroidal atrophy and alopecia syndrome 720850008 Coloboma, congenital heart disease, ichthyosiform dermatosis, intellectual disability ear anomaly syndrome 720639008 Dyskeratosis congenita 74911008 Ectodermal dysplasia and sensorineural deafness syndrome 732953008 Ectodermal dysplasia with ectrodactyly and macular dystrophy syndrome 720856002 Ectodermal dysplasia with hair-tooth defects 239027006 Ectodermal dysplasia with nail defect 239046007 Ectodermal dysplasia with natal teeth Turnpenny type 715576000 Ectodermal dysplasia with sweating defect 239048008 Ectodermal dysplasia, intellectual disability, central nervous system malformation syndrome 734017008 Ectodermal dysplasia-ocular malformation syndrome 31291009 Focal facial dermal dysplasia 789156003 Hereditary benign intraepithelial dyskeratosis 68897000 removed: 2003-07-31 Hypertrichosis cubiti 771181009 Hypotrichosis with juvenile macular degeneration syndrome 723364003 Ichthyosis, alopecia, eclabion, ectropion, intellectual disability syndrome 763404001 Johnson neuroectodermal syndrome 721584005 KID syndrome 239059004 Kirman syndrome 239038006 Lelis syndrome 719429003 Limb mammary syndrome 721972001 Lymphedema hypoparathyroidism syndrome 721083007 Odonto-tricho-ungual-digito-palmar syndrome 722063009 Oliver McFarlane syndrome 719944006 Oral-facial-digital syndrome 52868006 Papillon-Lefèvre syndrome 40158001 Scalp, ear, nipple syndrome 721888002 Skin fragility, wooly hair, palmoplantar keratoderma syndrome 778010006 Trichodysplasia with amelogenesis imperfecta syndrome 719911000 Trichothiodystrophy 723551003 Zlotogora Ogur syndrome 716248001 hierarchies a selection of possible paths
SNOMED CT Concept 138875005 Clinical finding 404684003 Integumentary system finding 106077005 Disorder of integument 128598002 Congenital anomaly of integument 38164009 Congenital anomaly of skin 199879009 Genodermatosis 239001006 Ectodermal dysplasia 8654005 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of embryonic structure 609521009 Congenital ectodermal defect 254154003 Ectodermal dysplasia 8654005 ancestors sorted most to least specific
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.
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