ORPHA:165655
Genetic intestinal disease
- Type
- Category
- Group
- Group of disorders
- Status
- active
This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Genetic intestinal disease | |
| fr | Maladie intestinale génétique | |
| de | Intestinale Krankheit, genetisch bedingte | |
| es | Enfermedad intestinal genética | |
| it | Malattia intestinale di origine genetica | |
| nl | Genetische darmziekte | |
| pt | Doença genética intestinal | |
| pl | Genetyczna choroba jelit | |
| cs | Geneticky podmíněná onemocnění střev | |
| uk | Генетично обумовлене кишкове захворювання | |
| zh | 遗传性肠道疾病 | |
| tr | Genetik bağırsak hastalığı |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 15616 | E | validated | |
| UMLS | C5680438 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
3
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:165652Rare genetic gastroenterological disease
rare genetic diseases
Children (16):
- ORPHA:1116Aplasia cutis congenita-intestinal lymphangiectasia syndrome
- ORPHA:435988Chronic atrial and intestinal dysrhythmia syndrome
- ORPHA:104007Congenital enteropathy involving intestinal mucosa development
- ORPHA:104006Congenital intestinal disease due to an enzymatic defect
- ORPHA:104003Congenital intestinal transport defect
- ORPHA:468635Cryptogenic multifocal ulcerous stenosing enteritis
- ORPHA:477787Cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder
- ORPHA:363306Genetic intestinal disease due to fat malabsorption
- ORPHA:363314Genetic intestinal polyposis
- ORPHA:363300Genetic intractable diarrhea of infancy
- ORPHA:104004Intestinal disease due to vitamin absorption anomaly
- ORPHA:104013Metabolic disease with intestinal involvement
- ORPHA:90362Primary intestinal lymphangiectasia
- ORPHA:365563Primary short bowel syndrome
- ORPHA:104009Rare disease involving intestinal motility
- ORPHA:104012Rare monogenic inflammatory bowel disease
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
0 recordsNo prevalence record in this release.
6
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/165655
- This record as JSON: /data/d/165655.json