Idiopathic gastroparesis
- Type
- Disease
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- Adolescent, Adult, Childhood, Elderly, Infancy
- Status
- active
A rare idiopathic gastroesophageal disease characterized by delayed gastric emptying in the absence of mechanical obstruction of the gastric outlet. Patients present symptoms including nausea, vomiting, early satiety, postprandial fullness, bloating, abdominal pain and, in more severe cases, dehydration, electrolyte disturbances, weight loss and malnutrition.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Idiopathic gastroparesis | |
| fr | Gastroparésie idiopathique | |
| de | Gastroparese, idiopathische | |
| es | Gastroparesia idiopática | |
| it | Gastroparesi idiopatica | |
| nl | Idiopathische gastroparese | |
| pt | Gastroparésia idiopática | |
| pl | Gastropareza idiopatyczna | |
| cs | Idiopatická gastroparéza | |
| uk | Ідіопатичний гастропарез | |
| zh | 特发性胃肌轻瘫 | |
| tr | İdiyopatik gastroparezi |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | K31.8 | NTBT | attributed | validated |
| ICD-11 | DA41.00 | E | specific | validated |
| MONDO | 0034150 | E | validated | |
| UMLS | C0267171 | 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
1 record| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Point prevalence | 1-5 / 10 000 | 11.4 / 100 000 | Specific population | Value and class | Validated | ORPHANET_30396519[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/558411
- This record as JSON: /data/d/558411.json