Congenital anomaly of skin   199879009

SNOMED CT code


SNOMED code199879009
nameCongenital anomaly of skin
statusactive
date introduced2002-01-31
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 morphologyMorphologically abnormal structure   49755003
Pathological processPathological developmental process   308490002
Finding siteSkin structure   39937001
OccurrenceCongenital   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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