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25319005: Chronic diarrhea of infants AND/OR young children (disorder)

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
42447011 Chronic diarrhea of infants AND/OR young children en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
196433013 Chronic diarrhoea of infants AND/OR young children en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
755623017 Chronic diarrhea of infants AND/OR young children (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
4471761000241116 diarrhée chronique du nourrisson et/ou du jeune enfant fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

6 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Chronic diarrhea of infants AND/OR young children Is a Chronic diarrhea true Inferred relationship Some
Chronic diarrhea of infants AND/OR young children Finding site Oesophagus, stomach, small intestine and large intestine together as a single entity. false Inferred relationship Some
Chronic diarrhea of infants AND/OR young children Has definitional manifestation Diarrhea false Inferred relationship Some
Chronic diarrhea of infants AND/OR young children Clinical course Chronic true Inferred relationship Some 3
Chronic diarrhea of infants AND/OR young children Interprets Bowel action false Inferred relationship Some 1
Chronic diarrhea of infants AND/OR young children Has interpretation Altered false Inferred relationship Some 1
Chronic diarrhea of infants AND/OR young children Finding site Intestinal structure true Inferred relationship Some 2
Chronic diarrhea of infants AND/OR young children Interprets Digestive system function false Inferred relationship Some 4
Inbound Relationships Type Active Source Characteristic Refinability Group
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. Is a True Chronic diarrhea of infants AND/OR young children Inferred relationship Some
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. Is a True Chronic diarrhea of infants AND/OR young children Inferred relationship Some
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. Is a True Chronic diarrhea of infants AND/OR young children Inferred relationship Some
Chronic diarrhea with villous atrophy is a rare, genetic gastroenterological disease characterized by the early onset of chronic diarrhea, vomiting, anorexia, lactic acidosis, renal insufficiency and hepatic involvement (mild elevation of liver enzymes, steatosis, hepatomegaly). Partial villous atrophy (with eosinophilic infiltration) is observed on intestinal biopsy. Although diarrhea may resolve, the development of neurologic symptoms (cerebellar ataxia, sensorineural deafness, seizures), retinitis pigmentosa and muscle weakness may complicate disease course and lead to death. There have been no further descriptions in the literature since 1994. Is a True Chronic diarrhea of infants AND/OR young children Inferred relationship Some
Congenital chronic diarrhoea with protein-losing enteropathy is a rare, genetic, intestinal disease characterised by early-onset, chronic, non-infectious, non-bloody, watery diarrhoea associated with protein-losing enteropathy which results in hypoalbuminaemia, hypogammaglobulinaemia and elevated stool alpha-1-antitrypsin. Patients typically present severe, intractable diarrhoea, failure to thrive, recurrent infections and oedema. Is a True Chronic diarrhea of infants AND/OR young children Inferred relationship Some
A rare, genetic, intestinal disease characterized by early-onset, chronic diarrhea and intestinal inflammation due to overactivity of guanylate cyclase 2C. Additional manifestations include meteorism, dehydration, metabolic acidosis and electrolyte disturbances. Intestinal dysmotility, small-bowel obstruction and esophagitis (with or without esophageal hernia), as well as irritable bowel syndrome (without severe abdominal pain) and Crohn's disease, are frequently associated. Is a True Chronic diarrhea of infants AND/OR young children Inferred relationship Some

This concept is not in any reference sets

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