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.

Cysts: Any fluid-filled closed cavity or sac that is lined by an EPITHELIUM. Cysts can be of normal, abnormal, non-neoplastic, or neoplastic tissues.

Fallopian Tubes: A pair of highly specialized muscular canals extending from the UTERUS to its corresponding OVARY. They provide the means for OVUM collection, and the site for the final maturation of gametes and FERTILIZATION. The fallopian tube consists of an interstitium, an isthmus, an ampulla, an infundibulum, and fimbriae. Its wall consists of three histologic layers: serous, muscular, and an internal mucosal layer lined with both ciliated and secretory cells.

Female:

Fistula: Abnormal communication most commonly seen between two internal organs, or between an internal organ and the surface of the body.

Male:

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.

Oviducts: Ducts that serve exclusively for the passage of eggs from the ovaries to the exterior of the body. In non-mammals, they are termed oviducts. In mammals, they are highly specialized and known as FALLOPIAN TUBES.

Vena Cava, Superior: The venous trunk which returns blood from the head, neck, upper extremities and chest.

Tooth: One of a set of bone-like structures in the mouth used for biting and chewing.

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.