Rectal disorder

disease
On this page

Also known as disease of rectumdisease or disorder of rectumdisorder of rectumrectum diseaserectum disease or disorder

Summary

Rectal disorder (MONDO:0001593) is a disease (an umbrella term covering 6 Mondo subtypes) and 2 clinical trials. A subtype of large intestine disorder — broader associated-gene and molecular evidence is on the parent page (see Disease family below).

At a glance

  • Umbrella term: 6 Mondo subtypes
  • Clinical trials: 2

Clinical features

No curated clinical features (Orphanet) for this disease.

Identifiers

Disease identifiers

FieldValue
Canonical namerectal disorder
Mondo IDMONDO:0001593
EFOEFO:0009685
MeSHD012002
DOIDDOID:1285
SNOMED CT5964004
UMLSC0034882
MedGen19701
Anatomy (UBERON)UBERON:0001052
Is cancer (heuristic)no

Also known as: disease of rectum · disease or disorder of rectum · disorder of rectum · rectal disorder · rectum disease · rectum disease or disorder

Disease family

An umbrella term covering 6 Mondo subtypes.

Classification path: disease › human disease › disease by body system or component › digestive system disorderintestinal disorder › large intestine disorder › rectal disorder

Related subtypes (10): anal canal cancer, colonic disorder, colorectal neoplasm, Crohn’s colitis, epithelial tumor of anal canal, shigellosis, polyp of large intestine, benign neoplasm of large intestine, colorectal Kaposi sarcoma, disorder of appendix

Subtypes (6): anal fistula, ulcer of anus and rectum, rectal neoplasm, anus disorder, rectal prolapse, polyp of rectum

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

Drugs indicated for this disease

2 approved, 1 in late-stage (phase 3) trials. Disease-direct ChEMBL indications, not inferred from the associated-gene cohort below.

DrugDevelopment status
CamphorApproved (phase 4)
LidocaineApproved (phase 4)
DexmedetomidinePhase 3 (in late-stage trials)

Clinical trials & evidence

Clinical trials

Clinical trials: 2.

Phase distribution (across all retrieved trials)

PhaseTrials
Not specified2

Top trials by phase / activity

NCTPhaseStatusTitle
NCT05368168Not specifiedRECRUITINGImpact of Early Postoperative Treatment With Posterior Tibial Nerve Stimulation on the Incidence and Duration of Low Anterior Rectal Resection Syndrome
NCT05231473Not specifiedCOMPLETEDImpact Of The Nurse Enhanced Recovery After Surgery Coordinator On The Compliance In Colorectal Surgery (nursERAS-BCN)

No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.