Persistence, persistent (congenital)

"Persistence, persistent (congenital)" References in the ICD-10-CM Index to Diseases and Injuries

References in the ICD-10-CM Index to Diseases and Injuries 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 - Q21.2 Atrioventricular septal defect
    • 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 - Q21.1 Atrial septal defect
      • ovale - Q21.1 Atrial septal defect
    • 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 - Q21.2 Atrioventricular septal defect
      • primum - Q21.2 Atrioventricular septal defect
      • secundum - Q21.1 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)

Applicable Clinical Terms Definitions

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.