Solitary rectal ulcer syndrome
- Type
- Disease
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- Adult
- Status
- active
Solitary rectal ulcer syndrome (SRUS) is a rare rectal disease characterized by rectal bleeding, abdominal pain, passage of mucus, sensation of incomplete evacuation, straining at defecation and rectal prolapse, secondary to ischemic changes in the rectum.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Solitary rectal ulcer syndrome | |
| fr | Syndrome de l'ulcère solitaire du rectum | |
| de | Solitary-rectal-ulcer-Syndrom | Rektumulkus, solitärer · Solitäres Geschwür des Rektums |
| es | Síndrome de úlcera rectal solitaria | |
| it | Sindrome dell'ulcera solitaria del retto | |
| nl | Solitaire rectale ulcus-syndroom | |
| pt | Síndrome úlcera retal solitária | |
| pl | Zespół samotnego wrzodu odbytnicy | |
| cs | Syndrom solitárního rektálního vředu | |
| uk | Синдром солітарної виразки прямої кишки | |
| zh | 孤立性直肠溃疡综合征 | |
| tr | Soliter rektal ülser sendromu |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | K62.6 | NTBT | attributed | validated |
| ICD-11 | DB33.0 | NTBT | index | validated |
| MONDO | 0016208 | E | validated | |
| UMLS | C4274343 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:117569Rare intestinal disease
rare gastroenterological diseases
No children.
Genes
0 directOrphanet records no gene directly on this code.
Prevalence and incidence
2 records| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Annual incidence | 1-9 / 100 000 | 1 / 100 000 | Europe | Value and class | Not yet validated | 18188027[PMID] |
| Point prevalence | Unknown | — | Worldwide | Class only | Not yet validated | ORPHANET |
Value is Orphadata's ValMoy: the mean estimate per 100 000 for prevalence and incidence, the number of cases or families for case reports.
HPO phenotypes
16 annotations · validated 2021-12-08| HPO | Term (as annotated by Orphanet) | Diagnostic |
|---|---|---|
| Very frequent (99-80%) | ||
| HP:0002573 | Hematochezia | |
| Frequent (79-30%) | ||
| HP:0002027 | Abdominal pain | |
| HP:0500005 | Anal pain | |
| HP:0012450 | Chronic constipation | |
| HP:0002254 | Intermittent diarrhea | |
| Occasional (29-5%) | ||
| HP:0000002 | Abnormality of body height | |
| HP:0012390 | Anal fissure | |
| HP:0001903 | Anemia | |
| HP:0025085 | Bloody diarrhea | |
| HP:0025086 | Bloody mucoid diarrhea | |
| HP:0000722 | Compulsive behaviors | |
| HP:0004325 | Decreased body weight | |
| HP:0002574 | Episodic abdominal pain | |
| HP:0002035 | Rectal prolapse | |
| HP:0012702 | Tenesmus | |
| Very rare (<4-1%) | ||
| HP:0012425 | Stercoral ulcer | |
Run the differential on the 1 obligate / very frequent terms
Annotation source: 31687110[PMID]_32097373[PMID]_29718850[PMID]
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/209964
- This record as JSON: /data/d/209964.json