Pediatric collagenous gastritis
Synonyms: Childhood-onset collagenous gastritis
- Type
- Disease
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- Adolescent, Childhood, Infancy
- Status
- active
A rare gastroenterologic disease characterized by the histopathological finding of a thickened (> 10 µm) gastric subepithelial collagen layer in association with an inflammatory infiltrate in the lamina propria. Patients typically present with upper abdominal pain and severe iron deficiency anemia. The condition is not commonly associated with autoimmune diseases, and involvement of the colon is less frequent than in the adult form. The disease takes a generally benign course with limited long-term morbidity and no increased mortality.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Pediatric collagenous gastritis | Childhood-onset collagenous gastritis |
| fr | Gastrite collagène pédiatrique | |
| de | Gastritis, kollagene, pädiatrische | Kollagene Gastritis des Kindes |
| es | Gastritis colagenosa pediátrica | Gastritis colagenosa de inicio en la infancia |
| it | Gastrite collagenosa pediatrica | |
| nl | Pediatrische collagene gastritis | Collagene gastritis met aanvang in de kindertijd |
| pt | Gastrite colagenosa pediátrica | |
| pl | Zapalenie kolagenowe żołądka wieku dziecięcego | Zapalenie kolagenowe żołądka o początku w wieku dziecięcym |
| cs | Dětská kolagenní gastritida | Kolagenní gastritida s nástupem v dětství |
| uk | Колагеновий гастрит у дітей | Колагеновий гастрит у дитячому віці |
| zh | 儿童胶原性胃炎 | = en |
| tr | Pediatrik kollajenöz gastrit | Çocuklukta başlayan kollajenöz gastrit |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | K29.6 | NTBT | attributed | validated |
| ICD-11 | DA42.Y | NTBT | attributed | validated |
| MONDO | 0044624 | E | validated | |
| UMLS | C5680109 | 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:101936Rare gastroesophageal 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 |
|---|---|---|---|---|---|---|
| Cases/families | 24 cases | Worldwide | Case(s) | Validated | 23538318[PMID]_25789098[PMID] | |
| Point prevalence | <1 / 1 000 000 | — | Worldwide | Class only | Validated | ORPHANET_25789098[PMID] |
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
Orphanet has no HPO annotation for this code in this release.
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/487809
- This record as JSON: /data/d/487809.json