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 anomaly of integument NOS
 * Congenital deformity of integument NOS

Q85 Phakomatoses, not elsewhere classified

 * Excludes1: ataxia telangiectasia [Louis-Bar] (G11.3)
 * familial dysautonomia [Riley-Day] (G90.1)
 * Q85.0 Neurofibromatosis (nonmalignant)
 * Von Recklinghausen's disease
 * Q85.1 Tuberous sclerosis
 * Bourneville's disease
 * Epiloia
 * Q85.8 Other phakomatoses, not elsewhere classified
 * Peutz-Jeghers Syndrome
 * Sturge-Weber(-Dimitri) syndrome
 * von Hippel-Lindau syndrome
 * Excludes1: Meckel-Gruber syndrome (Q61.9)
 * Q85.9 Phakomatosis, unspecified
 * Hamartosis NOS

Q86 Congenital malformation syndromes due to known exogenous causes, not elsewhere classified

 * Excludes2: iodine-deficiency-related hypothyroidism (E00-E02)
 * nonteratogenic effects of substances transmitted via placenta or breast milk (P04.-)
 * Q86.0 Fetal alcohol syndrome (dysmorphic)
 * Q86.1 Fetal hydantoin syndrome
 * Meadow's syndrome
 * Q86.2 Dysmorphism due to warfarin
 * Q86.8 Other congenital malformation syndromes due to known exogenous causes

Q87 Other specified congenital malformation syndromes affecting multiple systems

 * Use additional code(s) to identify all associated manifestations
 * Q87.0 Congenital malformation syndromes predominantly affecting facial appearance
 * Acrocephalopolysyndactyly
 * Acrocephalosyndactyly [Apert]
 * Cryptophthalmos syndrome
 * Cyclopia
 * Goldenhar syndrome
 * Moebius syndrome
 * Oro-facial-digital syndrome
 * Robin syndrome
 * Whistling face
 * Q87.1 Congenital malformation syndromes predominantly associated with short stature
 * Aarskog