This page needs to be proofread.
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
