Certain infectious and parasitic diseases
Certain infectious and parasitic diseases Certain infectious and parasitic diseases
Q84.9 Congenital malformation of integument, unspecified Congenital: · anomaly NOS · deformity NOS } of integument NOS Q85 Phakomatoses, not elsewhere classified Excludes: 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 Syndrome: · Peutz-Jeghers · Sturge-Weber(-Dimitri) · von Hippel-Lindau Excludes: Meckel-Gruber syndrome ( Q61.9 ) Q85.9 Phakomatosis, unspecified Hamartosis NOS Q86 Congenital malformation syndromes due to known exogenous causes, not elsewhere classified Excludes: 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 578 WHO’s ICD-10
Q87 Other specified congenital malformation syndromes affecting multiple systems Q87.0 Congenital malformation syndromes predominantly affecting facial appearance Acrocephalopolysyndactyly Acrocephalosyndactyly [Apert] Cryptophthalmos syndrome Cyclopia Syndrome: · Goldenhar · Moebius · oro-facial-digital · Robin Whistling face Q87.1 Congenital malformation syndromes predominantly associated with short stature Syndrome: · Aarskog · Cockayne · De Lange · Dubowitz · Noonan · Prader-Willi · Robinow-Silverman-Smith · Russell-Silver · Seckel · Smith-Lemli-Opitz Excludes: Ellis-van Creveld syndrome ( Q77.6 ) Q87.2 Congenital malformation syndromes predominantly involving limbs Syndrome: · Holt-Oram · Klippel-Trénaunay-Weber · nail patella · Rubinstein-Taybi · sirenomelia · thrombocytopenia with absent radius [TAR] · VATER Q87.3 Congenital malformation syndromes involving early overgrowth Syndrome: · Beckwith-Wiedemann · Sotos · Weaver Q87.4 Marfan's syndrome Q87.5 Other congenital malformation syndromes with other skeletal changes Version for 2007 579
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Q84.9 Congenital malformation of integument, unspecified<br />
Congenital:<br />
· anomaly NOS<br />
· deformity NOS } of integument NOS<br />
Q85 Phakomatoses, not elsewhere classified<br />
Excludes: ataxia telangiectasia [Louis-Bar] ( G11.3 )<br />
familial dysautonomia [Riley-Day] ( G90.1 )<br />
Q85.0 Neurofibromatosis (nonmalignant)<br />
Von Recklinghausen's disease<br />
Q85.1 Tuberous sclerosis<br />
Bourneville's disease<br />
Epiloia<br />
Q85.8 Other phakomatoses, not elsewhere classified<br />
Syndrome:<br />
· Peutz-Jeghers<br />
· Sturge-Weber(-Dimitri)<br />
· von Hippel-Lindau<br />
Excludes: Meckel-Gruber syndrome ( Q61.9 )<br />
Q85.9 Phakomatosis, unspecified<br />
Hamartosis NOS<br />
Q86 Congenital malformation syndromes due to known exogenous<br />
causes, not elsewhere classified<br />
Excludes: iodine-deficiency-related hypothyroidism ( E00-E02 )<br />
nonteratogenic effects of substances transmitted via placenta or breast<br />
milk ( P04.- )<br />
Q86.0 Fetal alcohol syndrome (dysmorphic)<br />
Q86.1 Fetal hydantoin syndrome<br />
Meadow's syndrome<br />
Q86.2 Dysmorphism due to warfarin<br />
Q86.8 Other congenital malformation syndromes due to known exogenous causes<br />
578 WHO’s ICD-10
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