Diarrheal disease secondary to altered bowel motility

Summary

Diarrheal disease secondary to altered bowel motility (MONDO:0000251) is a disease. A subtype of diarrheal disease — broader associated-gene and molecular evidence is on the parent page (see Disease family below).

Clinical features

No curated clinical features (Orphanet) for this disease.

Identifiers

Disease identifiers

Field	Value
Canonical name	diarrheal disease secondary to altered bowel motility
Mondo ID	MONDO:0000251
Is cancer (heuristic)	no

Also known as: diarrhea secondary to altered bowel motility · diarrhoea secondary to altered bowel motility · motility-related diarrhea · motility-related diarrhoea

Disease family

This is a subtype of diarrheal disease. Genetic, therapeutic, and trial evidence is largely curated at the broader-term level — see the parent page for the associated-gene cohort and molecular evidence.

Classification path: disease › human disease › disease by body system or component › digestive system disorder › diarrheal disease › diarrheal disease secondary to altered bowel motility

Related subtypes (6): secretory diarrhea, inflammatory diarrhea, acute diarrhea, congenital diarrhea, chronic diarrheal disease, non-infectious diarrheal disease

Subtypes (2): diarrheal disease secondary to increased bowel motility, diarrheal disease secondary to decreased bowel motility

Genetics & variants

GWAS landscape

No GWAS associations recorded — common-variant (GWAS) studies don’t cover this disease (typical for Mendelian / rare diseases). See the curated gene cohort and Mendelian overlap below.

Variant details and genetic-evidence tiers

No tiered GWAS variants or ClinVar records for this disease.

Genes & proteins

No associated-gene cohort resolved for this disease. Atlas builds the molecular and therapeutic sections — associated genes, protein families, druggability, pathways, interactions, and drug associations — by aggregating over a disease’s associated genes (resolved via GWAS / GenCC / ClinVar / CIViC), and none resolved here. This is expected for antibody-mediated, autoimmune, or otherwise non-gene-defined conditions; the curated evidence for this disease is its clinical features, GWAS susceptibility, and clinical trials (above).

Function

No pathway enrichment — requires an associated-gene cohort.

Therapeutics

No druggable-target or therapeutic data for this disease’s cohort.

Clinical trials & evidence

Clinical trials

Clinical trials: 0.