773579007: Congenital chronic diarrhea with protein-losing enteropathy (disorder)

• SNOMED CT Concept\Clinical finding (finding)\...
• \Viscus structure finding (finding)\Abdominal organ finding\Bowel finding\...
• \Finding of defecation\Finding of bowel action\Altered bowel function\Diarrheal disorder\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.
• \Finding of small intestine\Disorder of small intestine\Protein-losing enteropathy\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.
• \Disorder of intestine\Chronic diarrhea\Chronic diarrhea of infants AND/OR young children\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.
• \Disorder of intestine\Diarrheal disorder\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.
• \Disorder of intestine\Disorder of small intestine\Protein-losing enteropathy\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.
• \Digestive system finding (finding)\Gastrointestinal tract finding (finding)\Bowel finding\Finding of defecation\Finding of bowel action\Altered bowel function\Diarrheal disorder\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.
• \Digestive system finding (finding)\Gastrointestinal tract finding (finding)\Bowel finding\Finding of small intestine\Disorder of small intestine\Protein-losing enteropathy\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.
• \Digestive system finding (finding)\Gastrointestinal tract finding (finding)\Bowel finding\Disorder of intestine\Chronic diarrhea\Chronic diarrhea of infants AND/OR young children\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.
• \Digestive system finding (finding)\Gastrointestinal tract finding (finding)\Bowel finding\Disorder of intestine\Diarrheal disorder\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.
• \Digestive system finding (finding)\Gastrointestinal tract finding (finding)\Bowel finding\Disorder of intestine\Disorder of small intestine\Protein-losing enteropathy\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.
• \Digestive system finding (finding)\Gastrointestinal tract finding (finding)\Disorder of gastrointestinal tract (disorder)\Disorder of intestine\Chronic diarrhea\Chronic diarrhea of infants AND/OR young children\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.
• \Digestive system finding (finding)\Gastrointestinal tract finding (finding)\Disorder of gastrointestinal tract (disorder)\Disorder of intestine\Diarrheal disorder\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.
• \Digestive system finding (finding)\Gastrointestinal tract finding (finding)\Disorder of gastrointestinal tract (disorder)\Disorder of intestine\Disorder of small intestine\Protein-losing enteropathy\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.
• \Digestive system finding (finding)\Gastrointestinal tract finding (finding)\Disorder of gastrointestinal tract (disorder)\Malabsorption syndrome\Protein-losing enteropathy\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.
• \Digestive system finding (finding)\Diarrhea\Chronic diarrhea\Chronic diarrhea of infants AND/OR young children\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.
• \Digestive system finding (finding)\Diarrhea\Diarrheal disorder\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.
• \Digestive system finding (finding)\Disorder of digestive system (disorder)\Digestive system hereditary disorder\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.
• \Digestive system finding (finding)\Disorder of digestive system (disorder)\Chronic digestive system disorder\Chronic diarrhea\Chronic diarrhea of infants AND/OR young children\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.
• \Digestive system finding (finding)\Disorder of digestive system (disorder)\Disorder of digestive tract (disorder)\Disorder of gastrointestinal tract (disorder)\Disorder of intestine\Chronic diarrhea\Chronic diarrhea of infants AND/OR young children\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.
• \Digestive system finding (finding)\Disorder of digestive system (disorder)\Disorder of digestive tract (disorder)\Disorder of gastrointestinal tract (disorder)\Disorder of intestine\Diarrheal disorder\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.
• \Digestive system finding (finding)\Disorder of digestive system (disorder)\Disorder of digestive tract (disorder)\Disorder of gastrointestinal tract (disorder)\Disorder of intestine\Disorder of small intestine\Protein-losing enteropathy\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.
• \Digestive system finding (finding)\Disorder of digestive system (disorder)\Disorder of digestive tract (disorder)\Disorder of gastrointestinal tract (disorder)\Malabsorption syndrome\Protein-losing enteropathy\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.
• \Digestive system finding (finding)\Disorder of digestive system (disorder)\Disorder of digestive organ (disorder)\Disorder of intestine\Chronic diarrhea\Chronic diarrhea of infants AND/OR young children\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.
• \Digestive system finding (finding)\Disorder of digestive system (disorder)\Disorder of digestive organ (disorder)\Disorder of intestine\Diarrheal disorder\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.
• \Digestive system finding (finding)\Disorder of digestive system (disorder)\Disorder of digestive organ (disorder)\Disorder of intestine\Disorder of small intestine\Protein-losing enteropathy\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.
• \Digestive system finding (finding)\Disorder of digestive system (disorder)\Disorder of digestive system specific to fetus OR newborn\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.
• \Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Disorder of abdominopelvic segment of trunk\Disorder of abdomen (disorder)\Disorder of intestine\Chronic diarrhea\Chronic diarrhea of infants AND/OR young children\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.
• \Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Disorder of abdominopelvic segment of trunk\Disorder of abdomen (disorder)\Disorder of intestine\Diarrheal disorder\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.
• \Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Disorder of abdominopelvic segment of trunk\Disorder of abdomen (disorder)\Disorder of intestine\Disorder of small intestine\Protein-losing enteropathy\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.
• \Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of abdomen\Abdominal organ finding\Bowel finding\Finding of defecation\Finding of bowel action\Altered bowel function\Diarrheal disorder\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.
• \Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of abdomen\Abdominal organ finding\Bowel finding\Finding of small intestine\Disorder of small intestine\Protein-losing enteropathy\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.
• \Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of abdomen\Abdominal organ finding\Bowel finding\Disorder of intestine\Chronic diarrhea\Chronic diarrhea of infants AND/OR young children\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.
• \Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of abdomen\Abdominal organ finding\Bowel finding\Disorder of intestine\Diarrheal disorder\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.
• \Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of abdomen\Abdominal organ finding\Bowel finding\Disorder of intestine\Disorder of small intestine\Protein-losing enteropathy\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.
• \Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of abdomen\Disorder of abdomen (disorder)\Disorder of intestine\Chronic diarrhea\Chronic diarrhea of infants AND/OR young children\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.
• \Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of abdomen\Disorder of abdomen (disorder)\Disorder of intestine\Diarrheal disorder\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.
• \Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of abdomen\Disorder of abdomen (disorder)\Disorder of intestine\Disorder of small intestine\Protein-losing enteropathy\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.
• \Finding of trunk structure\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disorder of abdomen (disorder)\Disorder of intestine\Chronic diarrhea\Chronic diarrhea of infants AND/OR young children\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.
• \Finding of trunk structure\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disorder of abdomen (disorder)\Disorder of intestine\Diarrheal disorder\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.
• \Finding of trunk structure\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disorder of abdomen (disorder)\Disorder of intestine\Disorder of small intestine\Protein-losing enteropathy\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.
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Digestive system hereditary disorder\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.
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\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.
• \Disease\Fetal and/or neonatal disorder\Congenital disease\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.
• \Disease\Fetal and/or neonatal disorder\Disorder of digestive system specific to fetus OR newborn\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.
• \Disease\Disorder of body system\Hereditary disorder by system\Digestive system hereditary disorder\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.
• \Disease\Disorder of body system\Disorder of digestive system (disorder)\Digestive system hereditary disorder\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.
• \Disease\Disorder of body system\Disorder of digestive system (disorder)\Chronic digestive system disorder\Chronic diarrhea\Chronic diarrhea of infants AND/OR young children\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.
• \Disease\Disorder of body system\Disorder of digestive system (disorder)\Disorder of digestive tract (disorder)\Disorder of gastrointestinal tract (disorder)\Disorder of intestine\Chronic diarrhea\Chronic diarrhea of infants AND/OR young children\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.
• \Disease\Disorder of body system\Disorder of digestive system (disorder)\Disorder of digestive tract (disorder)\Disorder of gastrointestinal tract (disorder)\Disorder of intestine\Diarrheal disorder\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.
• \Disease\Disorder of body system\Disorder of digestive system (disorder)\Disorder of digestive tract (disorder)\Disorder of gastrointestinal tract (disorder)\Disorder of intestine\Disorder of small intestine\Protein-losing enteropathy\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.
• \Disease\Disorder of body system\Disorder of digestive system (disorder)\Disorder of digestive tract (disorder)\Disorder of gastrointestinal tract (disorder)\Malabsorption syndrome\Protein-losing enteropathy\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.
• \Disease\Disorder of body system\Disorder of digestive system (disorder)\Disorder of digestive organ (disorder)\Disorder of intestine\Chronic diarrhea\Chronic diarrhea of infants AND/OR young children\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.
• \Disease\Disorder of body system\Disorder of digestive system (disorder)\Disorder of digestive organ (disorder)\Disorder of intestine\Diarrheal disorder\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.
• \Disease\Disorder of body system\Disorder of digestive system (disorder)\Disorder of digestive organ (disorder)\Disorder of intestine\Disorder of small intestine\Protein-losing enteropathy\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.
• \Disease\Disorder of body system\Disorder of digestive system (disorder)\Disorder of digestive system specific to fetus OR newborn\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.
• \Disease\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disorder of abdomen (disorder)\Disorder of intestine\Chronic diarrhea\Chronic diarrhea of infants AND/OR young children\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.
• \Disease\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disorder of abdomen (disorder)\Disorder of intestine\Diarrheal disorder\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.
• \Disease\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disorder of abdomen (disorder)\Disorder of intestine\Disorder of small intestine\Protein-losing enteropathy\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.
• \Disease\Chronic disease\Chronic digestive system disorder\Chronic diarrhea\Chronic diarrhea of infants AND/OR young children\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.

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2019. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
5405308010	Congenital chronic diarrhea with protein-losing enteropathy is a rare, genetic, intestinal disease characterized by early-onset, chronic, non-infectious, non-bloody, watery diarrhea associated with protein-losing enteropathy which results in hypoalbuminemia, hypogammaglobulinemia and elevated stool alpha-1-antitrypsin. Patients typically present severe, intractable diarrhea, failure to thrive, recurrent infections and edema.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
5405309019	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.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
3724272019	Congenital chronic diarrhea with protein-losing enteropathy (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3724273012	Congenital chronic diarrhea with exudative enteropathy	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3724274018	Congenital chronic diarrhoea with protein-losing enteropathy	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3724275017	Congenital chronic diarrhea with protein-losing enteropathy	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3724276016	Congenital chronic diarrhoea with exudative enteropathy	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core

Expanded Value Set

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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