FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.22-SNAPSHOT  |  FHIR Version n/a  User: [n/a]

93032003: Congenital atresia of intestinal tract (disorder)


Status: current, 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
153881013 Congenital atresia of intestinal tract en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
153882018 Imperforate intestinal tract en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
836681018 Congenital atresia of intestinal tract (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5870401000241119 atrésie congénitale du tractus intestinal fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5870411000241117 atrésie congénitale de l'intestin fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


27 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital atresia of intestinal tract Is a Congenital anomaly of lower alimentary tract false Inferred relationship Some
Congenital atresia of intestinal tract Finding site Intestinal structure false Inferred relationship Some 2
Congenital atresia of intestinal tract Associated morphology Congenital atresia false Inferred relationship Some 1
Congenital atresia of intestinal tract Occurrence Congenital false Inferred relationship Some
Congenital atresia of intestinal tract Finding site Jejunum, ileum, colon, rectum, and anal canal false Inferred relationship Some 1
Congenital atresia of intestinal tract Is a Congenital anomaly of digestive tract false Inferred relationship Some
Congenital atresia of intestinal tract Associated morphology anomalie congénitale false Inferred relationship Some 1
Congenital atresia of intestinal tract Finding site Intestinal structure false Inferred relationship Some 1
Congenital atresia of intestinal tract Finding site Intestinal structure false Inferred relationship Some 2
Congenital atresia of intestinal tract Finding site Intestinal structure false Inferred relationship Some 1
Congenital atresia of intestinal tract Is a Congenital malformation false Inferred relationship Some
Congenital atresia of intestinal tract Occurrence Congenital false Inferred relationship Some
Congenital atresia of intestinal tract Is a Congenital anomaly of intestinal tract true Inferred relationship Some
Congenital atresia of intestinal tract Associated morphology Congenital atresia false Inferred relationship Some 1
Congenital atresia of intestinal tract Finding site Intestinal structure true Inferred relationship Some 1
Congenital atresia of intestinal tract Occurrence Congenital false Inferred relationship Some 2
Congenital atresia of intestinal tract Finding site Intestinal structure false Inferred relationship Some 2
Congenital atresia of intestinal tract Associated morphology Congenital atresia false Inferred relationship Some 2
Congenital atresia of intestinal tract Occurrence Congenital true Inferred relationship Some 1
Congenital atresia of intestinal tract Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Congenital atresia of intestinal tract Associated morphology Atresia (morphologic abnormality) true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Congenital atresia of colon Is a False Congenital atresia of intestinal tract Inferred relationship Some
Congenital atresia of small intestine Is a True Congenital atresia of intestinal tract Inferred relationship Some
Congenital atresia of rectum Is a False Congenital atresia of intestinal tract Inferred relationship Some
atrésies gastro-intestinales multiples Is a False Congenital atresia of intestinal tract Inferred relationship Some
Imperforate anus Is a False Congenital atresia of intestinal tract Inferred relationship Some
Atresia of large intestine (disorder) Is a True Congenital atresia of intestinal tract Inferred relationship Some
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. Is a True Congenital atresia of intestinal tract Inferred relationship Some
Neonatal intestinal perforation co-occurrent and due to intestinal atresia (disorder) Due to True Congenital atresia of intestinal tract Inferred relationship Some 3
Neonatal intestinal perforation co-occurrent and due to intestinal atresia (disorder) Is a True Congenital atresia of intestinal tract Inferred relationship Some
Fetal intrauterine intestinal perforation co-occurrent and due to congenital atresia of intestinal tract (disorder) Due to True Congenital atresia of intestinal tract Inferred relationship Some 3
Fetal intrauterine intestinal perforation co-occurrent and due to congenital atresia of intestinal tract (disorder) Is a True Congenital atresia of intestinal tract Inferred relationship Some
A rare, potentially fatal, genetic, visceral malformation syndrome characterized by neonatal diabetes, hypoplastic or annular pancreas, duodenal and jejunal atresia, as well as gallbladder aplasia or hypoplasia. Patients typically present intrauterine growth restriction, failure to thrive, malnutrition, intestinal malrotation, malabsorption, conjugated hyperbilirubinemia, acholia and infections. Cardiac anomalies may also be associated. Is a True Congenital atresia of intestinal tract Inferred relationship Some
Congenital atresia of intestine at multiple levels Is a True Congenital atresia of intestinal tract Inferred relationship Some
A rare genetic disease characterized by multiple intestinal atresia in association with combined immunodeficiency and inflammatory bowel disease. Clinical features include widespread atresia extending from the stomach to the rectum, homogenous calcifications in the abdominal cavity, hepatic cholestasis, cirrhosis, and chronic liver failure, hypoplastic thymus, and increased susceptibility to mainly bacteria and viruses. The immunological phenotype consists of profound generalized T-cell lymphopenia and milder natural killer cell and B-cell lymphopenia, as well as low serum levels of IgG, IgA, and IgM, with elevated serum IgE. The disease is mostly fatal in infancy or childhood. Is a True Congenital atresia of intestinal tract Inferred relationship Some
Multiple intestinal atresia is a rare form of intestinal atresia characterized by the presence of numerous atresic segments in the small bowel (duodenum) or large bowel and leading to symptoms of intestinal obstruction: vomiting, abdominal bloating and inability to pass meconium in newborns. Is a True Congenital atresia of intestinal tract Inferred relationship Some

This concept is not in any reference sets

Back to Start