aandoening van huid
congenitale afwijking van integumentum
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congenitale misvorming van huid (aandoening)
congenitale misvorming van huid
Congenital anomaly of skin
Congenital malformation of the skin
Congenital skin anomalies
Congenital cutaneous anomaly
Id199879009
StatusDefined
Associated morphologymorfologische afwijking
Finding sitestructuur van huid
Occurrencecongenitaal
Pathological processproces van pathologische ontwikkeling
General Practice / Family Practice reference set
DHD Diagnosethesaurus-referentieset
ICD-10 complex map reference set
TargetQ82.9
RuleTRUE
AdviceALWAYS Q82.9
CorrelationSNOMED CT source code to target map code correlation not specified
International Classification of Primary Care, Second edition complex map reference set
TargetS83
RuleTRUE
AdviceALWAYS S83
CorrelationSNOMED CT source code to target map code correlation not specified
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Acromegaloid phenotype with cutis verticis gyrata and corneal leukoma
Agammaglobulinemia, microcephaly, craniosynostosis, severe dermatitis syndrome
aplasia cutis congenita18
Arthrogryposis hyperkeratosis syndrome lethal form
Autosomal recessive cutis laxa type 2B
Brugsch's syndrome
Cavernous lymphangioma of skin
Congenital diffuse lipomatosis
Congenital erosive and vesicular dermatosis
Congenital fecal fistula
Congenital hamartoma of skin10
Congenital hyperplasia of sebaceous glands of lip
Congenital scar
congenitale afwijking van dermatoglyfenpatroon5
congenitale dermale sinus
congenitale misvorming van haar31
congenitale pigmentafwijkingen van huid17
congenitale vasculaire malformatie in huid7
Craniofaciofrontodigital syndrome
Cutaneous lesion resulting from spina bifida
Cutaneous lesion resulting from spinal dysraphism1
Cutis gyrata syndrome of Beare and Stevenson
Dermatoleukodystrophy
Double eyebrow
encefalocraniocutane lipomatose
Facial dysmorphism, cleft palate, loose skin syndrome
facomatose17
Focal dermal hypoplasia
focale dermale hypoplasie syndroom
gelokaliseerde huidatrofie van buikwand
Genodermatosis16
Haim Munk syndrome
Hennekam Beemer syndrome
Hereditary acantholytic dermatosis3
Hereditary benign intraepithelial dyskeratosis
incontinentia pigmenti
Intellectual disability, hypoplastic corpus callosum, preauricular tag syndrome
Intellectual disability, obesity, prognathism, eye and skin anomalies syndrome
LEOPARD-syndroom
Lumpy scalp syndrome
Macrostomia, preauricular tag, external ophthalmoplegia syndrome
MACS syndrome
Male emopamil-binding protein disorder with neurological defect
Median raphe cyst1
Microphthalmia with linear skin defect syndrome
Multiple pterygium syndrome3
naevus comedonicus
Osseous syndactyly of fingers - first web
Palmoplantar keratoderma, 46,XX sex reversal, predisposition to squamous cell carcinoma syndrome
porokeratosis actinica disseminata superficialis
Porokeratosis of Mibelli, linear unilateral type
Porokeratosis of Mibelli, plaque type
Porokeratosis of Mibelli, superficial disseminated type
Preauricular dimple
Severe dermatitis, multiple allergies, metabolic wasting syndrome
Simple syndactyly of fingers - first web
Simple syndactyly of fingers - second to fourth web
Spinocerebellar ataxia type 34
syndroom van Ehlers-Danlos23
syndroom van Kasabach-Merritt
Synophrys
teleangiectasia haemorrhagica hereditaria
Torticollis, keloids, cryptorchidism, renal dysplasia syndrome
Van den Bosch syndrome
webbed neck3
Webbed penis