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113276009: Intestinal 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
187095016 Intestinal tract en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
190711015 Intestines en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
190712010 Bowel en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
382650016 Intestinal structure en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
648155013 Intestinal structure (body structure) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
117631000087112 intestins fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
280481000077114 structure intestinale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
916791000172113 structure de l'intestin fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
948041000172111 intestin fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


479 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Intestinal structure Is a Intra-abdominal digestive structure true Inferred relationship Some
Intestinal structure Is a Oesophagus, stomach, small intestine and large intestine together as a single entity. true Inferred relationship Some
Intestinal structure partie de Entire abdomen (body structure) false Additional relationship Some
Intestinal structure partie de Entire gastrointestinal tract including esophagus, stomach and intestines false Additional relationship Some
Intestinal structure partie de A large organ in the thorax, abdomen, or pelvis false Additional relationship Some
Intestinal structure Is a Digestive organ structure false Inferred relationship Some
Intestinal structure Is a Jejunum, ileum, colon, rectum, and anal canal false Inferred relationship Some
Intestinal structure Is a Structure of organ within abdomen proper cavity (body structure) false Inferred relationship Some
Intestinal structure Is a Lower gastrointestinal tract part (body structure) false Inferred relationship Some
Intestinal structure Is a Structure of abdominopelvic viscus false Inferred relationship Some
Intestinal structure Is a Structure of intestine and/or mesentery (body structure) true Inferred relationship Some
Intestinal structure Is a Any organ (viscera) contained within the abdominopelvic cavity. The abdominopelvic viscera includes stomach, small intestine, large intestine, spleen, kidneys, adrenal glands, pancreas, liver and gallbladder and the viscera within the true pelvic cavity including ovaries, uterus, prostate, urinary bladder and anal canal. true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Neonatal intestinal perforation due to in utero intestinal volvulus (disorder) Finding site True Intestinal structure Inferred relationship Some 2
Neonatal intestinal perforation co-occurrent and due to in utero intraluminal obstruction (disorder) Finding site False Intestinal structure Inferred relationship Some 3
Neonatal intestinal perforation co-occurrent and due to in utero intraluminal obstruction (disorder) Finding site True Intestinal structure Inferred relationship Some 4
Chronic idiopathic non-infectious enteritis of intestine Finding site True Intestinal structure Inferred relationship Some 2
Neonatal perforation of intestine caused by drug (disorder) Finding site True Intestinal structure Inferred relationship Some 1
Infection of intestine caused by Vibrio (disorder) Finding site True Intestinal structure Inferred relationship Some 1
Diverticulitis of intestine (disorder) Finding site True Intestinal structure Inferred relationship Some 1
Diverticulosis of intestine Finding site False Intestinal structure Inferred relationship Some 1
Acute intestinal ischemia due to obstruction of vasculature of intestine (disorder) Finding site True Intestinal structure Inferred relationship Some 4
Gastrointestinal hypersensitivity caused by food (disorder) Finding site False Intestinal structure Inferred relationship Some 2
Closure of enterovesicovaginal fistula (procedure) Procedure site - Direct (attribute) True Intestinal structure Inferred relationship Some 4
Intestinal angioedema caused by angiotensin-converting enzyme inhibitor (disorder) Finding site True Intestinal structure Inferred relationship Some 1
Intestinal anastomosis present Finding site True Intestinal structure Inferred relationship Some 2
Intestinal bypass present Finding site True Intestinal structure Inferred relationship Some 2
Left hemicolectomy with stoma Procedure site - Direct (attribute) False Intestinal structure Inferred relationship Some 1
Right colectomy with stoma (procedure) Procedure site - Direct (attribute) False Intestinal structure Inferred relationship Some 3
Partial resection of colon with stoma (procedure) Procedure site - Direct (attribute) False Intestinal structure Inferred relationship Some 2
Neonatal candidiasis of intestine Finding site True Intestinal structure Inferred relationship Some 2
Nausea, vomiting and diarrhea Finding site True Intestinal structure Inferred relationship Some 2
Nervous diarrhea Finding site True Intestinal structure Inferred relationship Some 2
Raw-milk associated diarrhea Finding site True Intestinal structure Inferred relationship Some 2
Diarrhea due to diabetes mellitus Finding site True Intestinal structure Inferred relationship Some 2
Allergic diarrhea Finding site True Intestinal structure Inferred relationship Some 3
Postcholecystectomy diarrhea Finding site True Intestinal structure Inferred relationship Some 2
Non-infective diarrhea Finding site True Intestinal structure Inferred relationship Some 2
Diarrhea caused by alcohol intake (disorder) Finding site True Intestinal structure Inferred relationship Some 2
Dietetic diarrhea Finding site True Intestinal structure Inferred relationship Some 2
Inflammatory diarrhea Finding site True Intestinal structure Inferred relationship Some 2
Hemorrhagic diarrhea Finding site True Intestinal structure Inferred relationship Some 2
Diarrheic shellfish poisoning Finding site True Intestinal structure Inferred relationship Some 2
Diarrheal disorder Finding site True Intestinal structure Inferred relationship Some 2
Diarrhoea after gastrointestinal tract surgery Finding site False Intestinal structure Inferred relationship Some 3
Post-vagotomy diarrhoea Finding site True Intestinal structure Inferred relationship Some 2
Psychogenic diarrhea Finding site True Intestinal structure Inferred relationship Some 2
Diarrhea and vomiting after gastrointestinal tract surgery Finding site False Intestinal structure Inferred relationship Some 4
Antibiotic-associated diarrhea (disorder) Finding site True Intestinal structure Inferred relationship Some 2
Acute diarrhea (disorder) Finding site True Intestinal structure Inferred relationship Some 2
Brainerd diarrhea (disorder) Finding site True Intestinal structure Inferred relationship Some 2
Diarrhea caused by drug Finding site True Intestinal structure Inferred relationship Some 2
Trichohepatoenteric syndrome Finding site True Intestinal structure Inferred relationship Some 2
Non-infective neonatal diarrhea (disorder) Finding site False Intestinal structure Inferred relationship Some
Fetal intrauterine intestinal perforation co-occurrent and due to congenital stenosis of intestinal tract Finding site False Intestinal structure Inferred relationship Some 3
Fetal intrauterine intestinal perforation co-occurrent and due to congenital stenosis of intestinal tract Finding site False Intestinal structure Inferred relationship Some 4
Fetal intrauterine intestinal perforation co-occurrent and due to congenital atresia of intestinal tract (disorder) Finding site False Intestinal structure Inferred relationship Some 3
Fetal intrauterine intestinal perforation co-occurrent and due to congenital atresia of intestinal tract (disorder) Finding site False Intestinal structure Inferred relationship Some 4
Satoyoshi syndrome is a rare, multisystemic autoimmune disease mainly characterized by intermittent painful muscle spasms, alopecia (totalis or universalis in most cases) and long-lasting diarrhea that could lead to malnutrition, growth retardation, and amenorrhea. Secondary bone deformities and various endocrine anomalies may also be associated. Antinuclear antibodies are reported in many cases. Finding site True Intestinal structure Inferred relationship Some 2
Drug-induced constipation Finding site True Intestinal structure Inferred relationship Some 1
Chronic idiopathic constipation Finding site True Intestinal structure Inferred relationship Some 3
Obstipation Finding site True Intestinal structure Inferred relationship Some 2
Functional constipation Finding site True Intestinal structure Inferred relationship Some 2
Chronic constipation without overflow Finding site True Intestinal structure Inferred relationship Some 3
Chronic constipation Finding site True Intestinal structure Inferred relationship Some 2
Constipation due to spasm of colon (disorder) Finding site True Intestinal structure Inferred relationship Some 2
Constipation due to neurogenic bowel (disorder) Finding site True Intestinal structure Inferred relationship Some 2
Therapeutic opioid induced constipation (disorder) Finding site True Intestinal structure Inferred relationship Some 1
MRI of intestine Procedure site - Direct (attribute) True Intestinal structure Inferred relationship Some 1
Benign infantile seizures associated with mild gastroenteritis is a rare infantile epilepsy syndrome characterized by benign afebrile seizures in previously healthy infants and children (age range 1 month to 6 years) with mild acute gastroenteritis without any central nervous system infection, severe dehydration, or electrolyte imbalances. In most cases the seizures are tonic-clonic with focal origin on EEG, occur between day 1 and 6 following onset of acute gastroenteritis, cease within 24 hours and do not persist after the illness. Finding site True Intestinal structure Inferred relationship Some 3
Diarrhea in pregnancy Finding site True Intestinal structure Inferred relationship Some 1
Constipation alternates with diarrhea Finding site True Intestinal structure Inferred relationship Some 2
Chronic diarrhea Finding site True Intestinal structure Inferred relationship Some 2
Infectious diarrheal disease Finding site True Intestinal structure Inferred relationship Some 2
Intractable diarrhea-choanal atresia-eye anomalies syndrome is characterized by the association of intractable diarrhea of infancy with choanal atresia. Short stature, a prominent and broad nasal bridge, micrognathia, single palmar creases, chronic corneal inflammation, cytopenia, and abnormal hair texture were also reported. So far, the syndrome has been described in three children from the same family. The absence of intellectual deficit and immune deficiency allow this syndrome to be distinguished from other forms of intractable diarrhea of infancy described previously. Finding site True Intestinal structure Inferred relationship Some 5
Chronic diarrhea of unknown origin Finding site True Intestinal structure Inferred relationship Some 2
Diarrhea co-occurrent and due to carcinoid syndrome (disorder) Finding site True Intestinal structure Inferred relationship Some 1
A very rare genetic gastroenterological disease characterized by severe malabsorptive diarrhea (requiring parenteral nutrition and disappearing at fasting) due to a lack of intestinal enteroendocrine cells. It is associated with early-onset (within the first weeks of life) dehydration, metabolic acidosis and diabetes mellitus (that can develop until late childhood). Patient may display various degrees of pancreatic insufficiency that does not explain diarrhea, as it is not reduced with pancreatic enzyme supplementation. Central hypogonadism (developing in the second decade), as well as an association with celiac disease have been reported. Finding site True Intestinal structure Inferred relationship Some 1
A rare intestinal disease characterized by impaired absorption of starch and short polymers of glucose due to primary small intestinal glucoamylase deficiency. Patients present in infancy or early childhood with chronic diarrhea, abdominal distention, and bloating. Levels of pancreatic amylase are typically normal, and histopathological analysis shows normal morphology of the intestinal mucosa. Finding site True Intestinal structure Inferred relationship Some 1
Chronic diarrhea of infants AND/OR young children Finding site True Intestinal structure Inferred relationship Some 2
Non-infective neonatal diarrhea (disorder) Finding site True Intestinal structure Inferred relationship Some 2
Prototheca diarrhoea Finding site True Intestinal structure Inferred relationship Some 2
Traveler's diarrhea Finding site True Intestinal structure Inferred relationship Some 2
Epidemic diarrhea Finding site True Intestinal structure Inferred relationship Some 2
Chronic amoebiasis Finding site False Intestinal structure Inferred relationship Some 1
Complete obstruction of intestine Finding site False Intestinal structure Inferred relationship Some 1
Peutz-Jeghers polyps of small bowel Finding site False Intestinal structure Inferred relationship Some 3
Peutz-Jeghers syndrome Finding site False Intestinal structure Inferred relationship Some 2
Double incontinence Finding site False Intestinal structure Inferred relationship Some 1
Childhood double incontinence (finding) Finding site False Intestinal structure Inferred relationship Some 1
Acquired fructose intolerance Finding site False Intestinal structure Inferred relationship Some 1
Infantile gastroenteritis Finding site False Intestinal structure Inferred relationship Some 2
Nonbacterial gastroenteritis of infant Finding site False Intestinal structure Inferred relationship Some 2
Refractory celiac disease is a rare intestinal disease characterized by persistent or recurrent symptoms and signs of confirmed celiac disease despite a long-term, strict, gluten-free diet, in the absence of other causes of villous atrophy or malignant complications and with or without presence of increased abnormal intraepithelial lymphocytes. Finding site True Intestinal structure Inferred relationship Some 1
Familial omphalocele syndrome with facial dysmorphism is a rare genetic developmental defect during embryogenesis characterized by omphalocele associated with facial dysmorphism including flat face, short, upturned nose, long and wide philtrum and flattened maxillary arch and abnormalities of hands. Finding site True Intestinal structure Inferred relationship Some 1
Isosporiasis co-occurrent with human immunodeficiency virus infection (disorder) Finding site True Intestinal structure Inferred relationship Some 2
Chronic intestinal amoebiasis without abscess Finding site True Intestinal structure Inferred relationship Some 1
Crohn disease of anal canal (disorder) Finding site False Intestinal structure Inferred relationship Some 2
Inflammatory polyps co-occurrent and due to inflammatory bowel disease (disorder) Finding site False Intestinal structure Inferred relationship Some 2
A rare immune dysregulation disease with immunodeficiency characterized by severe, progressive infantile onset inflammatory bowel disease with pancolitis, perianal disease (ulceration, fistulae), recurrent respiratory, genitourinary and cutaneous infections, arthritis and a high risk of B-cell lymphoma. Finding site False Intestinal structure Inferred relationship Some 2
Chronic amoebiasis Finding site True Intestinal structure Inferred relationship Some 2
Bacterial dysentery Finding site True Intestinal structure Inferred relationship Some 2
Fetal intrauterine intestinal perforation co-occurrent and due to congenital atresia of intestinal tract (disorder) Finding site True Intestinal structure Inferred relationship Some 2
Fetal intrauterine intestinal perforation co-occurrent and due to congenital atresia of intestinal tract (disorder) Finding site True Intestinal structure Inferred relationship Some 1
A rare syndromic intestinal malformation characterized by ulcer formation in the umbilical cord associated with congenital upper-intestinal atresia, typically presenting with intra-uterine hemorrhaging from the ulcer site and subsequent fetal bradycardia. Finding site True Intestinal structure Inferred relationship Some 1
Neonatal intestinal perforation co-occurrent and due to intestinal atresia (disorder) Finding site True Intestinal structure Inferred relationship Some 2
Neonatal intestinal perforation co-occurrent and due to intestinal atresia (disorder) Finding site True Intestinal structure Inferred relationship Some 1
A rare multiple congenital anomaly syndrome characterized by flat face, hypertelorism, flat occiput, upward slanting palpebral fissures, cleft palate, micrognathia, short neck, and severe congenital heart defects. Malrotation of the intestine, bilateral clinodactyly, bilobed tongue, short fourth metatarsals and bifid thumbs may be additionally observed. Finding site True Intestinal structure Inferred relationship Some 2
Cryptosporidial gastroenteritis Finding site False Intestinal structure Inferred relationship Some 2
Intestinal obstruction co-occurrent and due to incisional hernia Finding site False Intestinal structure Inferred relationship Some 1
Ultrasound scan of bowel (procedure) Procedure site - Direct (attribute) True Intestinal structure Inferred relationship Some 1
Acquired pelvic enterocele Finding site False Intestinal structure Inferred relationship Some 1
Fistula of enterostomy (disorder) Finding site False Intestinal structure Inferred relationship Some 2
Neonatal inflammatory skin and bowel disease is a rare, life-threatening, autoinflammatory syndrome with immune deficiency disorder characterized by early-onset, life-long inflammation, affecting the skin and bowel, associated with recurrent infections. Patients present perioral and perianal psoriasiform erythema and papular eruption with pustules, failure to thrive associated with chronic malabsorptive diarrhea, intercurrent gastrointestinal infections and feeding troubles, as well as absent, short or broken hair and trichomegaly. Recurrent cutaneous and pulmonary infections lead to recurrent blepharitis, otitis externa and bronchiolitis. Finding site False Intestinal structure Inferred relationship Some 1

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