Congenital microgastria
- Type
- Morphological anomaly
- Group
- Disorder
- Age of onset
- Antenatal, Infancy, Neonatal
- Status
- active
Congenital microgastria is a rare malformation where the embryological development of the stomach is interrupted, leading to an abnormally small foregut in newborns and characterized by extreme feeding intolerance and malnutrition along with growth retardation and death if untreated. It is usually associated with multiple congenital anomalies.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Congenital microgastria | |
| fr | Microgastrie congénitale | |
| de | Mikrogastrie, kongenitale | |
| es | Microgastria congénita | |
| it | Microgastria congenita | |
| nl | Congenitale microgastrie | |
| pt | Microgastria congénita | |
| pl | Wrodzona mikrogastria | |
| cs | Vrozená mikrogastrie | |
| uk | Вроджена мікрогастрія | |
| zh | 先天性小胃 | |
| tr | Doğumsal mikrogastri |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | Q40.2 | NTBT | inclusion | validated |
| ICD-11 | LB13.Y | NTBT | index | validated |
| MONDO | 0016041 | E | validated | |
| UMLS | C0266150 | 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:108963Non-syndromic gastroduodenal malformation
rare developmental anomalies during embryogenesis; rare abdominal surgical 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 / 1 000 000 | — | Worldwide | Class only | Validated | ORPHANET_28361011[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/199293
- This record as JSON: /data/d/199293.json