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
  • 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
  • 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 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
  • 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 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
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