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Autosomal recessive early-onset inflammatory bowel disease
2 OMIM references -
4 associated genes
3 connected diseases
No signs/symptoms info
Disease Type of connection
Behçet disease
Multiple intestinal atresia
Split hand-split foot malformation
Synonym(s):
- Autosomal recessive early-onset IBD
Classification (Orphanet):
- Rare gastroenterologic disease
- Rare genetic disease
Classification (ICD10):
- Diseases of the digestive system -
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal recessive
External references:
2 OMIM references -
No MeSH references
Gene symbol UniProt reference OMIM reference
IL10 P22301124092
IL10RA Q13651146933
IL10RB Q08334123889
TTC7A Q9ULT0609332
No signs/symptoms info available.