Non-hypoproteinemic hypertrophic gastropathy
Synonyms: Hypertrophic gastropathy without hypoproteinemia
- Type
- Disease
- Group
- Disorder
- Inheritance
- Autosomal dominant
- Age of onset
- No data available
- Status
- active
A rare gastroesophageal disease characterized by diffusely enlarged gastric folds, excessive mucus secretion, normal serum protein and gastric TGF-alpha levels. Patients typically present anemia, abdominal pain not related to eating or bowel habits and absence of peripheral edema.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Non-hypoproteinemic hypertrophic gastropathy | Hypertrophic gastropathy without hypoproteinemia |
| fr | Gastropathie hypertrophique sans hypoprotéinémie | Gastrite hypertrophique sans perte de protéines |
| de | Hypertrophe Gastropathie, nicht-hypoproteinämische | Hypertrophe Gastropathie ohne Hypoproteinämie |
| es | Gastropatía hipertrófica no hipoproteinémica | Gastropatía hipertrófica sin hipoproteinemia |
| it | Gastropatia ipertrofica non ipoproteinemica | Gastropatia ipertrofica senza ipoproteinemia |
| nl | Niet-hypoproteïnemische hypertrofische gastropathie | Hypertrofische gastropathie zonder hypoproteïnemie |
| pt | Gastropatia hipertrófica não hipoproteinémica | |
| pl | Gastropatia przerostowa bez hipoproteinemii | Gastropatia przerostowa bez hipoproteinemii |
| cs | Non-hypoproteinemická hypertrofická gastropatie | Hypertrofická gastropatie bez hypoproteinemie |
| uk | Негіпопротеїнемічна гіпертрофічна гастропатія | Гіпертрофічна гастропатія без гіпопротеїнемії |
| zh | 非低蛋白性肥厚性胃病 | 肥厚性胃病不伴低蛋白血症 |
| tr | Hipoproteinemik olmayan hipertrofik gastropati | Hipoproteinemi ile seyretmeyen hipertrofik gastropati |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | K29.6 | NTBT | attributed | validated |
| ICD-11 | DA42.76 | NTBT | attributed | validated |
| MONDO | 0018009 | E | validated | |
| UMLS | C4750834 | 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 | 1 families | Worldwide | Family(ies) | Validated | 22711003[PMID] | |
| Point prevalence | <1 / 1 000 000 | — | Worldwide | Class only | 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
Orphanet has no HPO annotation for this code in this release.
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/329883
- This record as JSON: /data/d/329883.json