Home work?
Keep your critical coding and billing tools with you no matter where you work.
Create your Find-A-Code account today!
subscribe
Congenital anomaly of skin 199879009 SNOMED CT code SNOMED code 199879009 name Congenital anomaly of skin status active date introduced 2002-01-31 fully specified name(s) Congenital anomaly of skin (disorder) synonyms Congenital anomaly of skin Congenital cutaneous anomaly Congenital malformation of the skin Congenital skin anomalies attributes - group1 Associated morphology Morphologically abnormal structure 49755003 Pathological process Pathological developmental process 308490002 Finding site Skin structure 39937001 Occurrence Congenital 255399007 parents children [X]Other specified congenital malformations of skin 205976006 removed: 2009-01-31 Abnormal dermatoglyphic pattern 83145004 Acromegaloid phenotype with cutis verticis gyrata and corneal leukoma 403766000 Agammaglobulinemia, microcephaly, craniosynostosis, severe dermatitis syndrome 722281001 Aplasia cutis congenita 35484002 Arthrogryposis hyperkeratosis syndrome lethal form 726620005 Ash leaf spot, tuberous sclerosis 254243001 Autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis 765331004 Autosomal recessive cutis laxa type 2B 778068007 Blepharophimosis epicanthus inversus ptosis syndrome 715391004 Brugsch's syndrome 205570009 Cavernous lymphangioma of skin 254793001 CHILD syndrome 17608003 Congenital anomaly of hair 65033000 Congenital anomaly of nail 35964007 Congenital dermal sinus 70499005 Congenital erosive and vesicular dermatosis 773691007 Congenital extramedullary dermal hematopoiesis 1142089004 Congenital fecal fistula 204769001 Congenital hyperplasia of sebaceous glands of lip 27680009 Congenital infiltrating lipomatosis of face 1251402007 Congenital malformation of lymphatic vessel of skin 402809007 Congenital pigmentary anomaly of skin 59379005 removed: 2004-07-31 Congenital pigmentary skin anomalies 205564003 Congenital pigmented melanocytic nevus of skin 398943008 Congenital scar 74223008 Congenital skin fragility of animals 32840003 removed: 2014-01-31 Craniofaciofrontodigital syndrome 763320005 Cutaneous lesion resulting from spina bifida 403561007 Cutaneous vascular malformation 400042000 Cutis gyrata syndrome of Beare and Stevenson 703528008 Cutis laxa, x-linked 59399004 Dermatoleukodystrophy 733044009 Disseminated superficial actinic porokeratosis 41495000 Double eyebrow 253209004 Ehlers-Danlos and osteogenesis imperfecta syndrome 733457006 Ehlers-Danlos syndrome 398114001 Exostosis, anetoderma, brachydactyly type E syndrome 733416004 Facial dysmorphism, cleft palate, loose skin syndrome 763278004 Focal dermal hypoplasia 205573006 Francois syndrome 254150007 Genodermatosis 239001006 Haim Munk syndrome 719973009 Hereditary acantholytic dermatosis 254217002 Hereditary anetoderma 733467001 Hereditary benign intraepithelial dyskeratosis 400014002 Incontinentia pigmenti syndrome 205567005 removed: 2003-01-31 Intellectual disability, obesity, prognathism, eye and skin anomalies syndrome 774102003 Leprechaunism syndrome 111307005 MACS syndrome 723367005 Male emopamil-binding protein disorder with neurological defect 782739000 Median raphe cyst 782194002 Microphthalmia with linear skin defect syndrome 721879006 Multiple lentigines syndrome 111306001 Multiple pterygium syndrome 205819008 Neck webbing 11731003 Osseous syndactyly of fingers - first web 205142003 Other congenital skin anomalies 268286008 removed: 2010-01-31 Other specified skin anomalies 205559002 removed: 2010-01-31 Palmoplantar hyperkeratosis sclerodactyly syndrome 239076000 Palmoplantar keratoderma, 46,XX sex reversal, predisposition to squamous cell carcinoma syndrome 722202006 Preauricular dimple 1955003 Pulmonary tuberous sclerosis 233718008 Severe dermatitis, multiple allergies, metabolic wasting syndrome 774211005 Simple syndactyly of fingers - first web 205139009 Simple syndactyly of fingers - second to fourth web 205140006 Spinocerebellar ataxia type 34 719255000 Synophrys 253207002 Torticollis, keloids, cryptorchidism, renal dysplasia syndrome 771266007 Total congenital alopecia 311671002 removed: 2020-01-31 Unspecified congenital anomalies of skin 268292002 removed: 2010-01-31 Van den Bosch syndrome 733110004 Webbed penis 253852007 Werner syndrome 51626007 Wrinkly skin syndrome 238875009 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 SNOMED CT Concept 138875005 Clinical finding 404684003 Integumentary system finding 106077005 Skin finding 106076001 Disorder of skin 95320005 Congenital anomaly of skin 199879009 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.
Access to this feature is available in the following products:CPT® to SNOMED Crosswalks sign IN sign UP
Thank you for choosing Find-A-Code, please Sign In to remove ads.