Persistence, persistent (congenital) - in the ICD-10-CM Index

Browse the ICD-10-CM codes with references applicable to the clinical term "persistence, persistent (congenital)"

• Persistence, persistent (congenital)

  • anal membrane - Q42.3 Congenital absence, atresia and stenosis of anus without fistula

    • with fistula - Q42.2 Congenital absence, atresia and stenosis of anus with fistula

  • arteria stapedia - Q16.3 Congenital malformation of ear ossicles

  • atrioventricular canal - Q21.20 Atrioventricular septal defect, unspecified as to partial or complete

  • branchial cleft NOS - Q18.2 Other branchial cleft malformations

    • cyst - Q18.0 Sinus, fistula and cyst of branchial cleft

    • fistula - Q18.0 Sinus, fistula and cyst of branchial cleft

    • sinus - Q18.0 Sinus, fistula and cyst of branchial cleft

  • bulbus cordis in left ventricle - Q21.8 Other congenital malformations of cardiac septa

  • canal of Cloquet - Q14.0 Congenital malformation of vitreous humor

  • capsule (opaque) - Q12.8 Other congenital lens malformations

  • cilioretinal artery or vein - Q14.8 Other congenital malformations of posterior segment of eye

  • cloaca - Q43.7 Persistent cloaca

  • communication - See: Fistula, congenital;

  • convolutions

    • aortic arch - Q25.46 Tortuous aortic arch

    • fallopian tube - Q50.6 Other congenital malformations of fallopian tube and broad ligament

    • oviduct - Q50.6 Other congenital malformations of fallopian tube and broad ligament

    • uterine tube - Q50.6 Other congenital malformations of fallopian tube and broad ligament

  • double aortic arch - Q25.45 Double aortic arch

  • ductus arteriosus (Botalli) - Q25.0 Patent ductus arteriosus

  • fetal

    • circulation - P29.38 Other persistent fetal circulation

    • form of cervix (uteri) - Q51.828 Other congenital malformations of cervix

    • hemoglobin, hereditary (HPFH) - D56.4 Hereditary persistence of fetal hemoglobin [HPFH]

  • foramen

    • Botalli - Q21.12 Patent foramen ovale

    • ovale - Q21.12 Patent foramen ovale

  • Gartner's duct - Q52.4 Other congenital malformations of vagina

  • hemoglobin, fetal (hereditary) (HPFH) - D56.4 Hereditary persistence of fetal hemoglobin [HPFH]

  • hyaloid

    • artery (generally incomplete) - Q14.0 Congenital malformation of vitreous humor

    • system - Q14.8 Other congenital malformations of posterior segment of eye

  • hymen, in pregnancy or childbirth - See: Pregnancy, complicated by, abnormal, vulva;

  • lanugo - Q84.2 Other congenital malformations of hair

  • left

    • posterior cardinal vein - Q26.8 Other congenital malformations of great veins

    • root with right arch of aorta - Q25.49 Other congenital malformations of aorta

    • superior vena cava - Q26.1 Persistent left superior vena cava

  • Meckel's diverticulum - Q43.0 Meckel's diverticulum (displaced) (hypertrophic)

    • malignant - See: Table of Neoplasms, small intestine, malignant;

  • mucosal disease (middle ear) - See: Otitis, media, suppurative, chronic, tubotympanic;

  • nail (s), anomalous - Q84.6 Other congenital malformations of nails

  • omphalomesenteric duct - Q43.0 Meckel's diverticulum (displaced) (hypertrophic)

  • organ or site not listed - See: Anomaly, by site;

  • ostium

    • atrioventriculare commune - Q21.23 Complete atrioventricular septal defect

    • primum - Q21.20 Atrioventricular septal defect, unspecified as to partial or complete

    • secundum - Q21.11 Secundum atrial septal defect

  • ovarian rests in fallopian tube - Q50.6 Other congenital malformations of fallopian tube and broad ligament

  • pancreatic tissue in intestinal tract - Q43.8 Other specified congenital malformations of intestine

  • primary (deciduous)

    • teeth - K00.6 Disturbances in tooth eruption

    • vitreous hyperplasia - Q14.0 Congenital malformation of vitreous humor

  • pupillary membrane - Q13.89 Other congenital malformations of anterior segment of eye

  • rhesus (Rh) titer - See: Complication(s), transfusion, incompatibility reaction, Rh (factor);

  • right aortic arch - Q25.47 Right aortic arch

  • sinus

    • urogenitalis

      • female - Q52.8 Other specified congenital malformations of female genitalia

      • male - Q55.8 Other specified congenital malformations of male genital organs

    • venosus with imperfect incorporation in right auricle - Q26.8 Other congenital malformations of great veins

  • thymus (gland) (hyperplasia) - E32.0 Persistent hyperplasia of thymus

  • thyroglossal duct - Q89.2 Congenital malformations of other endocrine glands

  • thyrolingual duct - Q89.2 Congenital malformations of other endocrine glands

  • truncus arteriosus or communis - Q20.0 Common arterial trunk

  • tunica vasculosa lentis - Q12.2 Coloboma of lens

  • umbilical sinus - Q64.4 Malformation of urachus

  • urachus - Q64.4 Malformation of urachus

  • vitelline duct - Q43.0 Meckel's diverticulum (displaced) (hypertrophic)

Cloaca: A dilated cavity extended caudally from the hindgut. In adult birds, reptiles, amphibians, and many fishes but few mammals, cloaca is a common chamber into which the digestive, urinary and reproductive tracts discharge their contents. In most mammals, cloaca gives rise to LARGE INTESTINE; URINARY BLADDER; and GENITALIA.

Communication: The exchange or transmission of ideas, attitudes, or beliefs between individuals or groups.

Meckel Diverticulum: A congenital abnormality characterized by the outpouching or sac formation in the ILEUM. It is a remnant of the embryonic YOLK SAC in which the VITELLINE DUCT failed to close.

Urachus: An embryonic structure originating from the ALLANTOIS. It is a canal connecting the fetal URINARY BLADDER and the UMBILICUS. It is normally converted into a fibrous cord postnatally. When the canal fails to be filled and remains open (patent urachus), urine leaks through the umbilicus.

Vitelline Duct: The narrow tube connecting the YOLK SAC with the midgut of the EMBRYO; persistence of all or part of it in post-fetal life produces abnormalities, of which the commonest is MECKEL DIVERTICULUM.