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64033007: Kidney structure (body structure)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
106434018 Kidney en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
499745018 Kidney structure en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
803382011 Kidney structure (body structure) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1232523012 Renal structure en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
12261000077111 structure d'un rein fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
886611000172115 ren fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
911291000172114 structure du rein fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
927081000172118 rein fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
982061000172117 nephros fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
997031000172114 structure rénale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


274 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Kidney structure Is a Structure of intra-abdominal urinary tract false Inferred relationship Some
Kidney structure Is a Urinary tract includes entire kidney and the urinary tract proper which relate to the ureter, bladder and urethra. false Inferred relationship Some
Kidney structure Is a Structure of abdominopelvic viscus false Inferred relationship Some
Kidney structure partie de voies urinaires en entier false Inferred relationship Some
Kidney structure partie de Entire region of retroperitoneal space false Additional relationship Some
Kidney structure partie de Entire upper genitourinary tract false Additional relationship Some
Kidney structure partie de A large organ in the thorax, abdomen, or pelvis false Additional relationship Some
Kidney structure Is a Structure of upper urinary tract true Inferred relationship Some
Kidney structure Is a Retroperitoneal compartment structure (body structure) true Inferred relationship Some
Kidney structure Is a Structure of organ within abdomen proper cavity (body structure) true Inferred relationship Some
Kidney structure Is a Structure of urinary organ (body structure) true Inferred relationship Some
Kidney structure Laterality Side (qualifier value) true Inferred relationship Some
Kidney structure Is a Structure of lateral half of abdomen lateral to midsagittal plane false Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Renal washings (specimen) Specimen source topography True Kidney structure Inferred relationship Some 1
Light chain nephropathy due to multiple myeloma Finding site True Kidney structure Inferred relationship Some 2
Tuberculosis of kidney Finding site True Kidney structure Inferred relationship Some 2
néphropathie tuberculeuse Finding site False Kidney structure Inferred relationship Some 2
End stage renal disease due to hypertension (disorder) Finding site True Kidney structure Inferred relationship Some 3
Acute kidney injury caused by contrast agent (disorder) Finding site False Kidney structure Inferred relationship Some 4
Morphologic change of kidney due to chronic nephritic syndrome (disorder) Finding site True Kidney structure Inferred relationship Some 2
Chronic kidney disease mineral and bone disorder Finding site True Kidney structure Inferred relationship Some 2
Renal impairment caused by Polyomavirus (disorder) Finding site True Kidney structure Inferred relationship Some 1
Disorder of kidney co-occurrent with human immunodeficiency virus infection (disorder) Finding site True Kidney structure Inferred relationship Some 1
néoplasme carcinoïde malin du rein Finding site False Kidney structure Inferred relationship Some 2
Renal failure syndrome co-occurrent with human immunodeficiency virus infection Finding site True Kidney structure Inferred relationship Some 3
Nephropathy caused by BK polyomavirus (disorder) Finding site True Kidney structure Inferred relationship Some 1
Chronic kidney disease stage 5 on dialysis (disorder) Finding site True Kidney structure Inferred relationship Some 3
Chronic kidney disease stage 5 with transplant (disorder) Finding site True Kidney structure Inferred relationship Some 3
Anaemia co-occurrent and due to chronic kidney disease stage 3 Finding site True Kidney structure Inferred relationship Some 6
A rare familial renal cancer syndrome characterized by a predisposition for developing bilateral and multifocal classic type papillary renal cell carcinomas (formerly known as type 1 papillary renal cell carcinoma until the 2022 WHO classification of renal tumors). Finding site False Kidney structure Inferred relationship Some 1
Renal dysplasia co-occurrent with megalocystis and sirenomelia Finding site False Kidney structure Inferred relationship Some 1
Doppler ultrasonography of kidney (procedure) Procedure site - Direct (attribute) False Kidney structure Inferred relationship Some 3
Fibulo-ulnar hypoplasia-renal anomalies syndrome is characterized by fibulo-ulnar dysostosis with renal anomalies. It has been described in two siblings born to non-consanguinous parents. The syndrome is lethal at birth (respiratory failure). Clinical manifestations include ear and facial anomalies (including micrognathia), symmetrical shortness of long bones, fibular agenesis and hypoplastic ulna, oligosyndactyly, congenital heart defects, and cystic or hypoplastic kidney. It is transmitted as an autosomal recessive trait. Finding site True Kidney structure Inferred relationship Some 3
An extremely rare inherited tumor syndrome within the familial nonmedullary thyroid cancer group. Finding site False Kidney structure Inferred relationship Some 2
A rare rodent-borne, potentially severe, hemorrhagic disease caused by Old World Hantaviruses characterized by high fever, malaise, headache, myalgia, arthralgia, backache, abdominal pain, oliguria/renal failure and systemic hemorrhagic manifestations. Finding site True Kidney structure Inferred relationship Some 4
Percutaneous irreversible electroporation ablation of neoplasm of kidney using computed tomography guidance (procedure) Procedure site - Direct (attribute) True Kidney structure Inferred relationship Some 2
Percutaneous irreversible electroporation ablation of neoplasm of kidney using computed tomography guidance (procedure) Procedure site - Direct (attribute) True Kidney structure Inferred relationship Some 3
Malakoplakia of kidney Finding site True Kidney structure Inferred relationship Some 3
Joubert syndrome with renal defect is a rare subtype of Joubert syndrome and related disorders characterized by the neurological features of JS associated with renal disease, in the absence of retinopathy. Finding site True Kidney structure Inferred relationship Some 2
néphrose coocurrente avec et due au lupus érythémateux systémique Finding site False Kidney structure Inferred relationship Some 1
Single photon emission computed tomography of kidney using dimercaptosuccinic acid (procedure) Procedure site - Direct (attribute) False Kidney structure Inferred relationship Some 2
Single photon emission computed tomography using dimercaptosuccinic acid with computed tomography of kidney with contrast (procedure) Procedure site - Direct (attribute) True Kidney structure Inferred relationship Some 2
Single photon emission computed tomography using dimercaptosuccinic acid with computed tomography of kidney with contrast (procedure) Procedure site - Direct (attribute) True Kidney structure Inferred relationship Some 3
Transplantation of kidney and pancreas (procedure) Procedure site - Indirect (attribute) False Kidney structure Inferred relationship Some 3
Insertion of fiducial marker into kidney using computed tomography guidance (procedure) Procedure site - Indirect (attribute) True Kidney structure Inferred relationship Some 2
Insertion of fiducial marker into kidney using computed tomography guidance (procedure) Procedure site - Direct (attribute) True Kidney structure Inferred relationship Some 3
Ulbright-Hodes syndrome is characterized by renal dysplasia, growth retardation, phocomelia or mesomelia, radiohumeral fusion, rib abnormalities, anomalies of the external genitalia and a Potter-like facies. The syndrome has been described in three infants (one pair of siblings and an unrelated case), all of whom died shortly after birth from respiratory distress resulting from pulmonary hypoplasia and oligohydramnios caused by renal dysplasia. The mode of transmission appears to be autosomal recessive. Finding site False Kidney structure Inferred relationship Some 3
Calculous pyelonephritis Finding site False Kidney structure Inferred relationship Some 4
Chronic pyelonephritis Finding site True Kidney structure Inferred relationship Some 2
Chronic pyelonephritis without medullary necrosis Finding site False Kidney structure Inferred relationship Some 2
Familial non-obstructive reflux-associated chronic pyelonephritis Finding site True Kidney structure Inferred relationship Some 1
Fungal infection of kidney Finding site True Kidney structure Inferred relationship Some 2
Renal candidiasis (disorder) Finding site True Kidney structure Inferred relationship Some 2
Papillary thyroid carcinoma with renal papillary neoplasia (disorder) Finding site False Kidney structure Inferred relationship Some 3
Renal cell carcinoma of kidney except renal pelvis (disorder) Finding site True Kidney structure Inferred relationship Some 1
Primary renal dysplasia (disorder) Finding site False Kidney structure Inferred relationship Some 2
Secondary renal dysplasia (disorder) Finding site True Kidney structure Inferred relationship Some 1
Congenital hemorrhagic renal cyst (disorder) Finding site True Kidney structure Inferred relationship Some 1
Bilateral medullary sponge kidney (disorder) Finding site False Kidney structure Inferred relationship Some 3
Bilateral medullary sponge kidney (disorder) Finding site False Kidney structure Inferred relationship Some 4
Bilateral multicystic renal dysplasia (disorder) Finding site False Kidney structure Inferred relationship Some
Bilateral congenital primary hydronephrosis (disorder) Finding site False Kidney structure Inferred relationship Some 5
Aristolochic acid nephropathy (disorder) Finding site True Kidney structure Inferred relationship Some 1
Dent disease type 1 (disorder) Finding site False Kidney structure Inferred relationship Some 1
Dent disease type 2 (disorder) Finding site False Kidney structure Inferred relationship Some 1
Bartter syndrome type 4a (disorder) Finding site False Kidney structure Inferred relationship Some 4
A rare multiple congenital anomalies syndrome characterized by limb deficiencies and renal anomalies that include split hand-split foot malformation, renal agenesis, polycystic kidneys, uterine anomalies and severe mandibular hypoplasia. An autosomal recessive mode of inheritance has been suggested. Finding site False Kidney structure Inferred relationship Some 5
A spectrum of congenital malformative disorders characterized by the co-occurrence of distal limb anomalies (usually bilateral cleft feet and/or hands) and renal defects (e.g. unilateral or bilateral agenesis), that can be associated with a variety of other anomalies such as those of genitourinary tract (genital anomalies, ureteral hypoplasias, vesicoureteral reflux), abdominal well defects, intestinal atresias, and lung malformations. Familial cases have been reported in which an autosomal recessive inheritance was suspected. Finding site True Kidney structure Inferred relationship Some 2
A rare, severe, circulatory system disease characterized by premature, diffuse, severe atherosclerosis (including the aorta and renal, coronary, and cerebral arteries), sensorineural deafness, diabetes mellitus, progressive neurological deterioration with cerebellar symptoms and photomyoclonic seizures, and progressive nephropathy. Partial deficiency of mitochondrial complexes III and IV in the kidney and fibroblasts (but not in muscle) may be associated. There have been no further descriptions in the literature since 1994. Finding site False Kidney structure Inferred relationship Some
A rare syndrome of multiple congenital anomalies characterized by radial ray malformations, renal abnormalities (mild malrotation, ectopia, horseshoe kidney, renal hypoplasia, vesico-ureteral reflux, bladder diverticula), and ophthalmological abnormalities (mainly colobomas, but also microphthalmia, ptosis, and Duane anomaly). The phenotype overlaps with other SALL4-related disorders including Okihiro syndrome and Holt-Oram syndrome. Finding site False Kidney structure Inferred relationship Some 3
néoplasme carcinoïde malin du rein Finding site False Kidney structure Inferred relationship Some 1
A rare genetic disease characterized by the presence of Müllerian duct derivatives (rudimentary uterus, fallopian tubes, and atretic vagina) and other genital anomalies (cryptorchidism, micropenis) in male newborns, intestinal and pulmonary lymphangiectasia, protein-losing enteropathy, hepatomegaly, and renal anomalies. Postaxial polydactyly, facial dysmorphism (including broad nasal bridge, bulbous nasal tip, long and prominent upper lip with smooth philtrum, hypertrophic alveolar ridges, and mild retrognathia, among other features), and short limbs have also been described. The syndrome is fatal in infancy. Finding site False Kidney structure Inferred relationship Some 6
Cyst of kidney (disorder) Finding site True Kidney structure Inferred relationship Some 1
Pre-renal acute kidney injury caused by reduction in circulating blood volume, distinct from other potential causes of pre-renal acute kidney injury, e.g. sepsis, decreased arterial blood pressure. Finding site True Kidney structure Inferred relationship Some 3
Acute kidney injury caused by heart failure. Also known as Cardiorenal syndrome type 1. Finding site True Kidney structure Inferred relationship Some 4
Acute kidney injury due to sepsis (disorder) Finding site True Kidney structure Inferred relationship Some 3
Single photon emission computed tomography of kidney (procedure) Procedure site - Direct (attribute) True Kidney structure Inferred relationship Some 1
syndrome d'Okamoto Finding site False Kidney structure Inferred relationship Some 7
Chronic kidney disease developing de novo in a person who has previously donated a kidney for the purposes of kidney transplanataion. Finding site True Kidney structure Inferred relationship Some 3
Chronic kidney disease developing as a result of removal of kidney tissue (including partial nephrectomy and radical nephrectomy) for the treatment of renal tumor. Finding site True Kidney structure Inferred relationship Some 3
Chronic kidney disease associated with chronic infection. Finding site True Kidney structure Inferred relationship Some 2
Excision of neoplasm of kidney (procedure) Procedure site - Direct (attribute) True Kidney structure Inferred relationship Some 1
Chronic kidney disease due to traumatic loss of kidney (disorder) Finding site True Kidney structure Inferred relationship Some 2
Inherited distal renal tubular acidosis combined with sensorineural deafness. Finding site True Kidney structure Inferred relationship Some 1
Perlman syndrome is characterized principally by polyhydramnios, neonatal macrosomia, bilateral renal tumors (hamartomas with or without nephroblastomatosis), hypertrophy of the islets of Langerhans and facial dysmorphism. Finding site True Kidney structure Inferred relationship Some 2
A rare congenital urogenital anomaly characterized by the presence of double uterus (didelphys, bicornuate or septum-complete or partial), unilateral cervico-vaginal obstruction (obstructed hemivagina-communicant, not communicant or septate and unilateral cervical atresia) and ipsilateral renal anomalies (renal agenesis and/or other urinary tract anomalies). Patients are usually diagnosed at puberty after menarche due to recurrent severe dysmenorrhea, chronic pelvic pain, excessive foul smelling mucopurulent discharge, spotting and intermenstrual bleeding (depending on the existence of uterine or vaginal communications). Fever, dyspareunia, and a palpable abdominal, pelvic or vaginal mass (mucocolpos or pyocolpos) may also be present. Finding site True Kidney structure Inferred relationship Some 2
Perlman syndrome is characterized principally by polyhydramnios, neonatal macrosomia, bilateral renal tumors (hamartomas with or without nephroblastomatosis), hypertrophy of the islets of Langerhans and facial dysmorphism. Finding site False Kidney structure Inferred relationship Some 3
A rare autosomal dominant association characterized clinically by juvenile cataract associated with bilateral microcornea, and renal glucosuria without other renal tubular defects. Finding site False Kidney structure Inferred relationship Some 4
Percutaneous biopsy of kidney using computed tomography guidance (procedure) Procedure site - Indirect (attribute) False Kidney structure Inferred relationship Some 2
Percutaneous biopsy of kidney using computed tomography guidance (procedure) Procedure site - Direct (attribute) True Kidney structure Inferred relationship Some 3
Haemolytic uraemic syndrome with either a family history of haemolytic uraemic syndrome or a genetic mutation known to cause haemolytic uraemic syndrome, or both. Finding site True Kidney structure Inferred relationship Some 7
Percutaneous needle biopsy of kidney using fluoroscopic guidance (procedure) Procedure site - Indirect (attribute) False Kidney structure Inferred relationship Some 2
Percutaneous needle biopsy of kidney using fluoroscopic guidance (procedure) Procedure site - Direct (attribute) True Kidney structure Inferred relationship Some 3
Renal insufficiency (disorder) Finding site True Kidney structure Inferred relationship Some 2
Acute renal insufficiency (disorder) Finding site True Kidney structure Inferred relationship Some 2
Chronic renal insufficiency (disorder) Finding site True Kidney structure Inferred relationship Some 2
A rare autosomal dominant association characterized clinically by juvenile cataract associated with bilateral microcornea, and renal glucosuria without other renal tubular defects. Finding site True Kidney structure Inferred relationship Some 3
Glomerulopathy with fibronectin deposits 2 (disorder) Finding site False Kidney structure Inferred relationship Some 1
A very rare syndrome characterized by intellectual deficit, horseshoe kidney, and congenital heart defects. Finding site False Kidney structure Inferred relationship Some 5
Bilateral medullary sponge kidney (disorder) Finding site False Kidney structure Inferred relationship Some 1
Multinodular goiter - cystic kidney - polydactyly syndrome is a very rare syndrome characterized by the association of multinodular goiter, cystic renal disease and digital anomalies. Finding site False Kidney structure Inferred relationship Some 6
This syndrome is characterized by intrauterine growth retardation, renal dysgenesis and a unilobed or absent thymus. Finding site False Kidney structure Inferred relationship Some 3
SERKAL (SEx Reversion, Kidneys, Adrenal and Lung dysgenesis) syndrome is characterized by female to male sex reversal and developmental anomalies of the kidneys, adrenal glands and lungs. Finding site True Kidney structure Inferred relationship Some 4
SERKAL (SEx Reversion, Kidneys, Adrenal and Lung dysgenesis) syndrome is characterized by female to male sex reversal and developmental anomalies of the kidneys, adrenal glands and lungs. Finding site False Kidney structure Inferred relationship Some 6
Magnetic resonance imaging of kidney without contrast (procedure) Procedure site - Direct (attribute) True Kidney structure Inferred relationship Some 1
CT of kidney-ureter-bladder without contrast Procedure site - Direct (attribute) True Kidney structure Inferred relationship Some 5
A rare genetic disease characterized by intrauterine growth retardation, permanent neonatal diabetes mellitus, and congenital hypothyroidism. Additional manifestations include congenital glaucoma, hepatic disease (hepatitis, fibrosis, and cirrhosis), polycystic kidneys, exocrine pancreatic dysfunction, sensorineural hearing impairment, developmental delay, and mild facial dysmorphism (such as flat nasal bridge, epicanthal folds, long philtrum, and low-set ears), among others. Finding site True Kidney structure Inferred relationship Some 1
A rare monoclonal gammopathy characterized by renal proximal tubule dysfunction secondary to monoclonal kappa light chain deposits in proximal tubular cells. Clinical presentation is with variable chronic kidney disease, low molecular weight proteinuria, aminoaciduria, hyperphosphaturia, uricosuria, bicarbonaturia, and non-diabetic glycosuria. Renal phosphate and urate wasting may cause hypophosphatemia and hypouricemia. Finding site False Kidney structure Inferred relationship Some
Ultrasonography guided puncture of cyst of kidney Procedure site - Direct (attribute) True Kidney structure Inferred relationship Some 1
Hypoparathyroidism-sensorineural deafness-renal disease syndrome is a rare, clinically heterogeneous genetic disorder characterized by the triad of hypoparathyroidism (H), sensorineural deafness (D) and renal disease (R). Finding site True Kidney structure Inferred relationship Some 11
Gestational proteinuria without hypertension (disorder) Finding site False Kidney structure Inferred relationship Some 1
Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis without severe ocular involvement (FHHN) is a form of familial primary hypomagnesemia, characterized by recurrent urinary tract infections, nephrolithiasis, bilateral nephrocalcinosis, renal magnesium (Mg) wasting, hypercalciuria and kidney failure. Finding site False Kidney structure Inferred relationship Some 1
Neurofaciodigitorenal syndrome is a rare multiple developmental anomalies syndrome characterized by neurological abnormalities (including megalencephaly, hypotonia, intellectual disability, abnormal EEG), dysmorphic facial features (high prominent forehead, grooved nasal tip, ptosis, ear anomalies) and acrorenal defects (such as triphalangism, broad halluces, unilateral renal agenesis). Additionally, intrauterine growth restriction, short stature and congenital heart defects may be associated. There have been no further descriptions in the literature since 1997. Finding site False Kidney structure Inferred relationship Some 5
Neurofaciodigitorenal syndrome is a rare multiple developmental anomalies syndrome characterized by neurological abnormalities (including megalencephaly, hypotonia, intellectual disability, abnormal EEG), dysmorphic facial features (high prominent forehead, grooved nasal tip, ptosis, ear anomalies) and acrorenal defects (such as triphalangism, broad halluces, unilateral renal agenesis). Additionally, intrauterine growth restriction, short stature and congenital heart defects may be associated. There have been no further descriptions in the literature since 1997. Finding site True Kidney structure Inferred relationship Some 3

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Reference Sets

Lateralizable body structure reference set (foundation metadata concept)

Anatomy structure and entire association reference set (foundation metadata concept)

Anatomy structure and part association reference set (foundation metadata concept)

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