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
- Q21.0 Ventricular septal defect
- Q21.1 Atrial septal defect
- Q22.1 Congenital pulmonary valve stenosis
- 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
- 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
- Q66.22 Congenital metatarsus adductus
- Q74.1 Congenital malformation of knee
- Q82.2 Mastocytosis
- Q85.02 Neurofibromatosis, type 2
- Q85.1 Tuberous sclerosis
- Q85.9 Phakomatosis, unspecified
- Q87.81 Alport syndrome
- Q89.2 Congenital malformations of other endocrine glands
- Q89.3 Situs inversus
- Q89.8 Other specified congenital malformations
- 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
- 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