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Hydronephrosis

Index Hydronephrosis

Hydronephrosis describes urine-filled dilation of the renal pelvis and/or calyces as a result of obstruction. [1]

65 relations: Abdominal mass, Abdominal pain, Anterograde pyelography, Aseem Shukla, Azotemia, Benign prostatic hyperplasia, Berdon syndrome, Bernhard Bardenheuer, Bladder augmentation, Bladder exstrophy, C16orf95, Calculus (medicine), Carcinogenic parasite, Cleft lip and cleft palate, Cri du chat syndrome, Cystinuria, Cystography, Dioxins and dioxin-like compounds, Distal 18q-, Duplicated ureter, Emergency ultrasound, Familial renal disease in animals, Fetal surgery, Fraley syndrome, ICD-10 Chapter XIV: Diseases of the genitourinary system, IgG4-related disease, Index of oncology articles, Ketamine, Kidney, Kidney stone disease, List of diseases (H), List of fetal abnormalities, List of ICD-9 codes 580–629: diseases of the genitourinary system, List of MeSH codes (C12), NAA15, Nephrostomy, Potter sequence, Preureteric vena cava, Pulmonary hypoplasia, Pyonephrosis, Renal biopsy, Renal cyst, Renal function, Renal pelvis, Renal ultrasonography, Ring 18, Robinow syndrome, Sacrococcygeal teratoma, Schinzel–Giedion syndrome, Schistosoma haematobium, ..., Schistosomiasis, Splenosis, Triploid syndrome, Ureter, Urethral stricture, Urinary retention, Urofacial syndrome, Uterine fibroid, Vesicoureteral reflux, Voiding cystourethrography, Wertheim-Meigs operation, 13q deletion syndrome, 2,3,7,8-Tetrachlorodibenzodioxin, 2p15-16.1 microdeletion syndrome, 3C syndrome. Expand index (15 more) »

Abdominal mass

An abdominal mass is any localized enlargement or swelling in the human abdomen.

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Abdominal pain

Abdominal pain, also known as a stomach ache, is a symptom associated with both non-serious and serious medical issues.

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Anterograde pyelography

Anterograde pyelography is the procedure used to visualize the upper collecting system of the urinary tract, i.e., kidney and ureter.

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Aseem Shukla

Aseem Ravindra Shukla is the Director of Minimally Invasive Surgery in the Department of Urology at the Children's Hospital of Philadelphia, PA and is an Associate Professor of Surgery (Urology) at the Perelman School of Medicine at the University of Pennsylvania.

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Azotemia

Azotemia (azot, "nitrogen" + -emia, "blood condition") is a medical condition characterized by abnormally high levels of nitrogen-containing compounds (such as urea, creatinine, various body waste compounds, and other nitrogen-rich compounds) in the blood.

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Benign prostatic hyperplasia

Benign prostatic hyperplasia (BPH), also called prostate enlargement, is a noncancerous increase in size of the prostate.

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Berdon syndrome

Berdon syndrome, also called Megacystis-microcolon-intestinal hypoperistalsis syndrome (MMIH syndrome), is an autosomal recessive fatal genetic disorder affecting newborns.

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Bernhard Bardenheuer

Bernhard Bardenheuer (July 12, 1839, Lamersdorf – August 13, 1913) was a German surgeon.

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Bladder augmentation

Bladder augmentation is a surgical alteration of the urinary bladder.

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Bladder exstrophy

Bladder exstrophy (also known as ectopia vesicae) is a congenital anomaly that exists along the spectrum of the exstrophy-epispadias complex and most notably involves protrusion of the urinary bladder through a defect in the abdominal wall.

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C16orf95

Chromosome 16 open reading frame 95 (C16orf95) is a gene which in humans encodes the protein C16orf95.

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Calculus (medicine)

A calculus (plural calculi), often called a stone, is a concretion of material, usually mineral salts, that forms in an organ or duct of the body.

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Carcinogenic parasite

Carcinogenic parasite is a parasitic organism which depends on other organisms (called hosts) for their survival, and cause cancer in such hosts.

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Cleft lip and cleft palate

Cleft lip and cleft palate, also known as orofacial cleft, is a group of conditions that includes cleft lip (CL), cleft palate (CP), and both together (CLP).

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Cri du chat syndrome

Cri du chat syndrome, also known as chromosome 5p deletion syndrome, 5p− syndrome (pronounced "five P minus") or Lejeune's syndrome, is a rare genetic disorder due to chromosome deletion on chromosome 5.

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Cystinuria

Cystinuria is an inherited autosomal recessive disease that is characterized by high concentrations of the amino acid cysteine in the urine, leading to the formation of cystine stones in the kidneys, ureter, and bladder.

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Cystography

In radiology and urology, a cystography is a procedure used to visualise the urinary bladder.

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Dioxins and dioxin-like compounds

Dioxins and dioxin-like compounds (DLCs) are compounds that are highly toxic environmental persistent organic pollutants (POPs).

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Distal 18q-

Distal 18q- is a genetic condition caused by a deletion of genetic material within one of the two copies of chromosome 18.

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Duplicated ureter

Duplicated ureter or Duplex Collecting System is a congenital condition in which the ureteric bud, the embryological origin of the ureter, splits (or arises twice), resulting in two ureters draining a single kidney.

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Emergency ultrasound

Emergency ultrasound or point-of-care ultrasound (POCUS) is the application of ultrasound at the point of care to make immediate patient-care decisions.

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Familial renal disease in animals

Familial renal disease is an uncommon cause of renal failure (kidney failure) in dogs and cats.

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Fetal surgery

Fetal surgery also known as Fetal reconstructive surgery antenatal surgery, prenatal surgery.

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Fraley syndrome

Fraley syndrome is a condition where the superior infundibulum of the upper calyx of the kidney is obstructed by the crossing renal (upper or middle section) artery branch, causing distension and dilatation of the calyx and presenting clinically as haematuria and nephralgia (ipsilateral flank pain).

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ICD-10 Chapter XIV: Diseases of the genitourinary system

ICD-10 is an international statistical classification used in health care and related industries.

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IgG4-related disease

IgG4-related disease (IgG4-RD), formerly known as IgG4-related systemic disease, is a chronic inflammatory condition characterized by tissue infiltration with lymphocytes and IgG4-secreting plasma cells, various degrees of fibrosis (scarring) and a usually prompt response to oral steroids.

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Index of oncology articles

This is a list of terms related to oncology.

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Ketamine

Ketamine, sold under the brand name Ketalar among others, is a medication mainly used for starting and maintaining anesthesia.

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Kidney

The kidneys are two bean-shaped organs present in left and right sides of the body in vertebrates.

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Kidney stone disease

Kidney stone disease, also known as urolithiasis, is when a solid piece of material (kidney stone) occurs in the urinary tract.

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List of diseases (H)

This is a list of diseases starting with the letter "H".

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List of fetal abnormalities

Fetal abnormalities are conditions that affect a fetus or embryo and may be fatal or cause disease after birth.

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List of ICD-9 codes 580–629: diseases of the genitourinary system

10.

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List of MeSH codes (C12)

The following is a list of the "C" codes for MeSH.

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NAA15

N-alpha-acetyltransferase 15, NatA auxiliary subunit also known as gastric cancer antigen Ga19 (GA19), NMDA receptor-regulated protein 1 (NARG1), and Tbdn100 is a protein that in humans is encoded by the NAA15 gene.

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Nephrostomy

A nephrostomy is an artificial opening created between the kidney and the skin which allows for the urinary diversion directly from the upper part of the urinary system (renal pelvis).

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Potter sequence

Potter sequence is the atypical physical appearance of a baby due to oligohydramnios experienced when in the uterus.

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Preureteric vena cava

A preureteric vena cava, also known as a retrocaval ureter, is a rare congenital malformation of the right human ureter, in which the ureter passes behind the inferior vena cava, causing compression possibly leading to hydronephrosis.

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Pulmonary hypoplasia

Pulmonary hypoplasia is incomplete development of the lungs, resulting in an abnormally low number or size of bronchopulmonary segments or alveoli.

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Pyonephrosis

Pyonephrosis (Greek pyon "pus" + nephros "kidney") is an infection of the kidneys' collecting system.

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Renal biopsy

Renal biopsy (also kidney biopsy) is a medical procedure in which a small piece of kidney is removed from the body for examination, usually under a microscope.

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Renal cyst

A renal cyst or kidney cyst, is a fluid collection in or on the kidney.

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Renal function

Renal function, in nephrology, is an indication of the kidney's condition and its role in renal physiology.

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Renal pelvis

The renal pelvis or pelvis of the kidney is the basin-like or funnel-like dilated proximal part of the ureter in the kidney.

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Renal ultrasonography

Renal ultrasonography (Renal US) is the examination of one or both kidneys using medical ultrasound.

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Ring 18

Ring 18 is a genetic condition caused by a deletion of the two tips of chromosome 18 followed by the formation of a ring-shaped chromosome.

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Robinow syndrome

Robinow syndrome is an extremely rare genetic disorder characterized by short-limbed dwarfism, abnormalities in the head, face, and external genitalia, as well as vertebral segmentation.

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Sacrococcygeal teratoma

Sacrococcygeal teratoma (SCT) is a type of tumor known as a teratoma that develops at the base of the coccyx (tailbone) and is thought to be derived from the primitive streak.

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Schinzel–Giedion syndrome

Schinzel–Giedion syndrome is a congenital neurodegenerative terminal syndrome.

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Schistosoma haematobium

Schistosoma haematobium (urinary blood fluke) is species of digenetic trematode, belonging to a group (genus) of blood flukes (Schistosoma).

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Schistosomiasis

Schistosomiasis, also known as snail fever and bilharzia, is a disease caused by parasitic flatworms called schistosomes.

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Splenosis

Splenosis is the result of spleen tissue breaking off the main organ and implanting at another site inside the body.  This is called ''heterotopic autotransplantation'' of the spleen.  It most commonly occurs as a result of traumatic splenic rupture or abdominal surgery.

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Triploid syndrome

Triploid syndrome, also called triploidy, is an extremely rare chromosomal disorder, in which a fetus has three copies of every chromosome instead of the normal two.

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Ureter

In human anatomy, the ureters are tubes made of smooth muscle fibers that propel urine from the kidneys to the urinary bladder.

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Urethral stricture

A urethral stricture is a narrowing of the urethra caused by injury, instrumentation, infection and certain non-infectious forms of urethritis.

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Urinary retention

Urinary retention is an inability to completely empty the bladder.

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Urofacial syndrome

Urofacial syndrome, or hydronephrosis with peculiar facial expression, is an autosomal recessive congenital disorder characterized by inverted facial expressions in association with obstructive disease of the urinary tract.

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Uterine fibroid

Uterine fibroids, also known as uterine leiomyomas or fibroids, are benign smooth muscle tumors of the uterus.

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Vesicoureteral reflux

Vesicoureteral reflux (VUR), also known as vesicoureteric reflux, is a condition in which urine flows retrograde, or backward, from the bladder into the ureters/kidneys.

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Voiding cystourethrography

In urology, voiding cystourethrography (VCUG) is a technique for visualizing a person's urethra and urinary bladder while the person urinates (voids).

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Wertheim-Meigs operation

The Wertheim-Meigs operation (named after Ernst Wertheim and Joe Vincent Meigs) is a surgical procedure for the treatment of cervical cancer performed by way of an abdominal incision.

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13q deletion syndrome

13q deletion syndrome is a rare genetic disease caused by the deletion of some or all of the large arm of human chromosome 13.

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2,3,7,8-Tetrachlorodibenzodioxin

2,3,7,8-Tetrachlorodibenzo-p-dioxin (TCDD) is a polychlorinated dibenzo''-p-''dioxin (sometimes shortened, though inaccurately, to simply "dioxin") with the chemical formula.

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2p15-16.1 microdeletion syndrome

2p15-16.1 microdeletion is a rare genetic disorder caused by a small deletion in the short arm of human chromosome 2.

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3C syndrome

3C syndrome, also known as CCC dysplasia, Craniocerebellocardiac dysplasia or Ritscher–Schinzel syndrome, is a rare condition, whose symptoms include heart defects, cerebellar hypoplasia, and cranial dysmorphism.

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Hydronephritis, Hydronephrotic, Hydroureteronephrosis, Ureterohydronephrosis.

References

[1] https://en.wikipedia.org/wiki/Hydronephrosis

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