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 Autosomal recessive cutis laxa type 2B 778068007 Brugsch's syndrome 205570009 Congenital anomaly of hair 65033000 Congenital dermal sinus 70499005 Congenital diffuse lipomatosis 238904008 Congenital erosive and vesicular dermatosis 773691007 Congenital fecal fistula 204769001 Congenital hamartoma of skin 400083002 Congenital hyperplasia of sebaceous glands of lip 27680009 Congenital pigmentary anomaly of skin 59379005 removed: 2004-07-31 Congenital pigmentary skin anomalies 205564003 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 syndrome 398114001 Encephalocraniocutaneous lipomatosis 238905009 Erythrokeratodermia variabilis 70041004 Facial dysmorphism, cleft palate, loose skin syndrome 763278004 Focal dermal hypoplasia 205573006 Francois syndrome 254150007 Genodermatosis 239001006 Haim Munk syndrome 719973009 Hennekam Beemer syndrome 722453009 Hereditary acantholytic dermatosis 254217002 Hereditary benign intraepithelial dyskeratosis 400014002 Incontinentia pigmenti syndrome 205567005 removed: 2003-01-31 Incontinentia pigmenti syndrome 367520004 Intellectual disability, hypoplastic corpus callosum, preauricular tag syndrome 722455002 Intellectual disability, obesity, prognathism, eye and skin anomalies syndrome 774102003 Kasabach-Merritt syndrome 86635005 Leprechaunism syndrome 111307005 Macrostomia, preauricular tag, external ophthalmoplegia syndrome 723366001 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 Neurocutaneous syndrome 78572006 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 keratoderma, 46,XX sex reversal, predisposition to squamous cell carcinoma syndrome 722202006 Porokeratosis of Mibelli, linear unilateral type 9031009 Porokeratosis of Mibelli, plaque type 20110000 Porokeratosis of Mibelli, superficial disseminated type 30005005 Preauricular dimple 1955003 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 hierarchies a selection of possible paths
SNOMED CT Concept 138875005 Clinical finding 404684003 Finding by site 118234003 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 Finding by site 118234003 Integumentary system finding 106077005 Skin finding 106076001 Disorder of skin 95320005 Congenital anomaly of skin 199879009 ancestors sorted most to least specific
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