ORPHA:183625
Rare genetic diabetes mellitus
- 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 | Rare genetic diabetes mellitus | |
| fr | Diabète sucré d'origine génétique | |
| de | Diabetes mellitus, genetisch bedingter, seltener | |
| es | Diabetes mellitus rara de origen genético | |
| it | Diabete mellito genetico raro | |
| nl | Zeldzame genetische diabetes mellitus | |
| pt | Diabetes mellitus genéticos raros | |
| pl | Rzadka postać cukrzycy uwarunkowana genetycznie | |
| cs | Vzácné dědičné typy diabetes mellitus | |
| uk | Рідкісний генетично обумовлений цукровий діабет | |
| zh | 罕见遗传性糖尿病 | |
| tr | Nadir genetik diabetes mellitus |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 15967 | E | validated | |
| UMLS | C5680537 | 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:156638Rare genetic endocrine disease
rare genetic diseases
Children (21):
- ORPHA:1133AREDYLD syndrome
- ORPHA:64Alström syndrome
- ORPHA:544628Atypical Fanconi syndrome-neonatal hyperinsulinism syndrome
- ORPHA:676Autosomal dominant hereditary chronic pancreatitis
- ORPHA:725898Bone marrow failure-diabetes mellitus syndrome
- ORPHA:168569H syndrome
- ORPHA:93111HNF1B-related autosomal dominant tubulointerstitial kidney disease
- ORPHA:3044Intellectual disability-dysmorphism-hypogonadism-diabetes mellitus syndrome
- ORPHA:445062Juvenile-onset diabetes mellitus-central and peripheral neurodegeneration syndrome
- ORPHA:552MODY
- ORPHA:2596Myopathy and diabetes mellitus
- ORPHA:224Neonatal diabetes mellitus
- ORPHA:2255Pancreatic hypoplasia-diabetes-congenital heart disease syndrome
- ORPHA:306558Primary microcephaly-epilepsy-permanent neonatal diabetes syndrome
- ORPHA:391408Primary microcephaly-mild intellectual disability-young-onset diabetes syndrome
- ORPHA:181368Rare insulin-resistance syndrome
- ORPHA:49827Thiamine-responsive megaloblastic anemia syndrome
- ORPHA:1667Wolcott-Rallison syndrome
- ORPHA:3463Wolfram syndrome
- ORPHA:411590Wolfram-like syndrome
- ORPHA:3464Woodhouse-Sakati syndrome
Codes that Orphanet moved or referred to this one:
- ORPHA:28455OBSOLETE: Pancreatic beta cell agenesis with neonatal diabetes mellitus referred to · inactive
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/183625
- This record as JSON: /data/d/183625.json