Intestinal obstruction

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
INTESTINAL OBSTRUCTION
C0021843
ACTG2 Causal — Disgenet
SLC26A3 Causal — Disgenet
INTESTINAL PSEUDO-OBSTRUCTION
C0021847MESH:D007418
CLMP Causal — CTD, Disgenet —
INTESTINAL PSEUDOOBSTRUCTION, NEURONAL, CHRONIC IDIOPATHIC, X-LINKED
300048MONDO:0010232
FLNA Causal
8644737 23037936 18854860
ClinVar, GWAS catalog, HPO
All12 Causal4 Unknown9
Related Diseases Diseases that share the most curated genes with Intestinal obstruction.
5 View disease cluster →
Visceral neuropathy 3 shared genesERBB3, ACTG2, TYMP Related via 3 shared genes including ERBB3, ACTG2, TYMP. Congenital short bowel syndrome 2 shared genesFLNA, CLMP Related via 2 shared genes including FLNA, CLMP. Congenital secretory diarrhea 2 shared genesSLC9A3, SLC26A3 Related via 2 shared genes including SLC9A3, SLC26A3. hemochromatosis type 1 1 shared geneHFE Related via 1 shared gene including HFE. Congenital idiopathic intestinal pseudoobstruction 1 shared geneFLNA Related via 1 shared gene including FLNA.