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ERNICA - European Reference Network for rare Inherited and Congenital Anomalies

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.

Related Structures

UOC Chirurgia Pediatrica
UOC Chirurgia Generale 1
UOC Anestesia e Rianimazione
UOC Dietetica e Nutrizione Clinica
UOC Nefrologia Pediatrica
UOC Patologia Neonatale
UOC Anatomia Patologica 2
UOC Gastroenterologia
UOC Clinica Pediatrica
UOC Clinica di Oncoematologia Pediatrica
UOC Otorinolaringoiatria
UOC Clinica Ginecologica Ostetrica
UOC Istituto Radiologia
UOSD Pneumologia e Allergologia Pediatrica

Desease list

Code ORPHACode ERNDenomination
RIG020Congenital enteropathies
Congenital hiatus hernia
Diaphragm eventratio
Pancreatic disease
.Eosinophilic esophagitis
ORPHA:104008RNG252Short bowel syndrome
ORPHA:104009Rare disease involving intestinal motility
ORPHA:10401RB0050Intestinal polyposis
ORPHA:104012Rare inflammatory bowel disease
ORPHA:1199Esophageal atresia
ORPHA:1203Duodenal and small bowel atresia
ORPHA:2140Congenital diaphragmatic hernia
ORPHA:2141Diaphragmatic defect-limb deficiency-skull defect syndrome
ORPHA:2290RI0070Microvillus inclusion disease
ORPHA:2368RN0320Gastroschisis
ORPHA:2736RN0322Lethal omphalocele-cleft palate syndrome
ORPHA:280403RN0322Familial omphalocele syndrome with facial dysmorphism
ORPHA:2847Pericardial and diaphragmatic defect
ORPHA:294422RNG252Intestinal failure
ORPHA:2978RI0040Chronic Intestinal Pseudo-Obstruction
ORPHA:3164RNG091Omphalocele syndrome, Shprintzen-Goldberg type
ORPHA:329242RIG020Congenital chronic diarrhea with protein-losing enteropathy
ORPHA:363306RIG020 Genetic intestinal disease due to fat malabsorption
ORPHA:388Hirschsprung disease
ORPHA:391673Necrotizing enterocolitis
ORPHA:401945Moyamoya disease with early-onset achalasia
ORPHA:494421Sacrococcygeal teratome
ORPHA:496693RN0322Omphalocele-diaphragmatic hernia-cardiovascular anomalies-radial ray defect syndrome
ORPHA:527468Diaphragmatic hernia-short bowel-asplenia syndrome
ORPHA:660RN0322Omphalocele  
ORPHA:73014RIG020Intractable diarrhea of infancy
ORPHA:73247Congenital esophageal stenosis
ORPHA:733RB0050Familial adenomatous polyposis
ORPHA:92050Epithelial dysplasia
ORPHA:930Achalasia
ORPHA:99777Achalasia-alacrimia syndrome