ERNICA addresses congenital malformations and diseases that appear early in life and require multidisciplinary care and long-term follow-up, and examines the transition to adulthood.
The network is organised around two main work streams in line with ORPHANET classifications and ICD10. One work stream deals with malformations of the digestive system and the other deals with malformations of the diaphragm and abdominal wall. In the latter work stream, there are working groups covering malformations of the oesophagus and a group working on gastroenterological and intestinal diseases. This group also includes a sub-group specialising in intestinal failure. Each working group has its own disease-specific task forces.
For some of these rare diseases, mortality rates can be as high as 50 %. ERNICA aims to improve the quality of care that patients receive and to reduce the long-term impact of these rare diseases in infants. The network will facilitate research collaborations with the power to develop evidence-based guidelines. Access to new surgical techniques and treatments will also be improved. ERNICA is a meeting place for national patients’ associations and caregivers, including nurses and other professions committed to improving patient outcomes.
Code ORPHA | Code ERN | Denomination |
---|---|---|
RIG020 | Congenital enteropathies | |
Congenital hiatus hernia | ||
Diaphragm eventratio | ||
Pancreatic disease | ||
. | Eosinophilic esophagitis | |
ORPHA:104008 | RNG252 | Short bowel syndrome |
ORPHA:104009 | Rare disease involving intestinal motility | |
ORPHA:10401 | RB0050 | Intestinal polyposis |
ORPHA:104012 | Rare inflammatory bowel disease | |
ORPHA:1199 | Esophageal atresia | |
ORPHA:1203 | Duodenal and small bowel atresia | |
ORPHA:2140 | Congenital diaphragmatic hernia | |
ORPHA:2141 | Diaphragmatic defect-limb deficiency-skull defect syndrome | |
ORPHA:2290 | RI0070 | Microvillus inclusion disease |
ORPHA:2368 | RN0320 | Gastroschisis |
ORPHA:2736 | RN0322 | Lethal omphalocele-cleft palate syndrome |
ORPHA:280403 | RN0322 | Familial omphalocele syndrome with facial dysmorphism |
ORPHA:2847 | Pericardial and diaphragmatic defect | |
ORPHA:294422 | RNG252 | Intestinal failure |
ORPHA:2978 | RI0040 | Chronic Intestinal Pseudo-Obstruction |
ORPHA:3164 | RNG091 | Omphalocele syndrome, Shprintzen-Goldberg type |
ORPHA:329242 | RIG020 | Congenital chronic diarrhea with protein-losing enteropathy |
ORPHA:363306 | RIG020 | Genetic intestinal disease due to fat malabsorption |
ORPHA:388 | Hirschsprung disease | |
ORPHA:391673 | Necrotizing enterocolitis | |
ORPHA:401945 | Moyamoya disease with early-onset achalasia | |
ORPHA:494421 | Sacrococcygeal teratome | |
ORPHA:496693 | RN0322 | Omphalocele-diaphragmatic hernia-cardiovascular anomalies-radial ray defect syndrome |
ORPHA:527468 | Diaphragmatic hernia-short bowel-asplenia syndrome | |
ORPHA:660 | RN0322 | Omphalocele |
ORPHA:73014 | RIG020 | Intractable diarrhea of infancy |
ORPHA:73247 | Congenital esophageal stenosis | |
ORPHA:733 | RB0050 | Familial adenomatous polyposis |
ORPHA:92050 | Epithelial dysplasia | |
ORPHA:930 | Achalasia | |
ORPHA:99777 | Achalasia-alacrimia syndrome |