Intestinal failure or congenital diarrhoeaGene: IL37
Single family reported with homozygous truncating variant this gene and infantile-onset of IBD, some functional data.
Created: 27 Apr 2021, 2:28 p.m.
Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal
Infantile inflammatory bowel disease
gene: IL37 was added gene: IL37 was added to Intestinal failure. Sources: Literature Mode of inheritance for gene: IL37 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: IL37 were set to 33674380 Phenotypes for gene: IL37 were set to Infantile inflammatory bowel disease Review for gene: IL37 was set to RED