5-Minute Clinical Consult
- Q01.9 Encephalocele, unspecified
- Q04.8 Other specified congenital malformations of brain
- Q05.0 Cervical spina bifida with hydrocephalus
- Q05.1 Thoracic spina bifida with hydrocephalus
- Q05.2 Lumbar spina bifida with hydrocephalus
- Q05.3 Sacral spina bifida with hydrocephalus
- Q05.4 Unspecified spina bifida with hydrocephalus
- Q05.5 Cervical spina bifida without hydrocephalus
- Q05.6 Thoracic spina bifida without hydrocephalus
- Q05.7 Lumbar spina bifida without hydrocephalus
- Q05.8 Sacral spina bifida without hydrocephalus
- Q05.9 Spina bifida, unspecified
- Q07.00 Arnold-Chiari syndrome without spina bifida or hydrocephalus
- Q07.01 Arnold-Chiari syndrome with spina bifida
- Q07.02 Arnold-Chiari syndrome with hydrocephalus
- Q14.1 Congenital malformation of retina
- Q18.0 Sinus, fistula and cyst of branchial cleft
- Q18.1 Preauricular sinus and cyst
- Q21.2 Atrioventricular septal defect
- Q22.1 Congenital pulmonary valve stenosis
- Q23.0 Congenital stenosis of aortic valve
- Q23.2 Congenital mitral stenosis
- Q23.3 Congenital mitral insufficiency
- Q24.8 Other specified congenital malformations of heart
- Q24.9 Congenital malformation of heart, unspecified
- Q25.0 Patent ductus arteriosus
- Q25.1 Coarctation of aorta
- Q33.4 Congenital bronchiectasis
- Q39.3 Congenital stenosis and stricture of esophagus
- Q40.0 Congenital hypertrophic pyloric stenosis
- Q41.9 Congen absence, atresia and stenosis of sm int, part unsp
- Q43.1 Hirschsprung's disease
- Q43.3 Congenital malformations of intestinal fixation
- Q43.8 Other specified congenital malformations of intestine
- Q50.2 Congenital torsion of ovary
- Q52.4 Other congenital malformations of vagina
- Q53.10 Unspecified undescended testicle, unilateral
- Q53.11 Abdominal testis, unilateral
- Q53.12 Ectopic perineal testis, unilateral
- Q53.20 Undescended testicle, unspecified, bilateral
- Q53.21 Abdominal testis, bilateral
- Q53.22 Ectopic perineal testis, bilateral
- Q53.9 Undescended testicle, unspecified
- Q61.11 Cystic dilatation of collecting ducts
- Q61.19 Other polycystic kidney, infantile type
- Q61.1 Polycystic kidney, infantile type
- Q61.2 Polycystic kidney, adult type
- Q61.3 Polycystic kidney, unspecified
- Q61.4 Renal dysplasia
- Q61.5 Medullary cystic kidney
- Q61.8 Other cystic kidney diseases
- Q62.0 Congenital hydronephrosis
- Q63.9 Congenital malformation of kidney, unspecified
- Q66.22 Congenital metatarsus adductus
- Q66.89 Other specified congenital deformities of feet
- Q68.6 Discoid meniscus
- Q74.1 Congenital malformation of knee
- Q82.0 Hereditary lymphedema
- Q82.2 Mastocytosis
- Q85.02 Neurofibromatosis, type 2
- Q85.1 Tuberous sclerosis
- Q85.9 Phakomatosis, unspecified
- Q87.40 Marfan's syndrome, unspecified
- Q87.410 Marfan's syndrome with aortic dilation
- Q87.418 Marfan's syndrome with other cardiovascular manifestations
- Q87.42 Marfan's syndrome with ocular manifestations
- Q87.43 Marfan's syndrome with skeletal manifestation
- Q87.81 Alport syndrome
- Q89.2 Congenital malformations of other endocrine glands
- Q89.3 Situs inversus
- Q89.8 Other specified congenital malformations
- Q90.0 Trisomy 21, nonmosaicism (meiotic nondisjunction)
- Q90.1 Trisomy 21, mosaicism (mitotic nondisjunction)
- Q90.2 Trisomy 21, translocation
- Q90.9 Down syndrome, unspecified
- Q90 Down syndrome
- Q96.0 Karyotype 45, X
- Q96.1 Karyotype 46, X iso (Xq)
- Q96.2 Karyotype 46, X w abnormal sex chromosome, except iso (Xq)
- Q96.3 Mosaicism, 45, X/46, XX or XY
- Q96.4 Mosaic, 45, X/other cell line(s) w abnormal sex chromosome
- Q96.8 Other variants of Turner's syndrome
- Q96.9 Turner's syndrome, unspecified
- Q98.0 Klinefelter syndrome karyotype 47, XXY
- Q98.1 Klinefelter syndrome, male with more than two X chromosomes
- Q98.3 Other male with 46, XX karyotype
- Q98.4 Klinefelter syndrome, unspecified
- Q98.5 Karyotype 47, XYY