ORPHA:181368
Rare insulin-resistance syndrome
- 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 insulin-resistance syndrome | |
| fr | Syndrome rare de résistance à l'insuline | |
| de | Seltenes Insulinresistenz-Syndrom | |
| es | Síndrome raro de resistencia a la insulina | |
| it | Sindrome rara da insulino-resistenza | |
| nl | Zeldzaam insulineresistentiesyndroom | |
| pt | Síndrome de resistência à insulina | |
| pl | Rzadki zespół oporny na insulinę | |
| cs | Vzácný syndrom inzulinové rezistence | |
| uk | Рідкісний синдром інсулінорезистентності | |
| zh | 罕见胰岛素抵抗综合征 | |
| tr | Nadir görülen insülin direnci sendromu |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-11 | 5A44 | NTBT | specific | validated |
| MONDO | 15885 | E | validated | |
| UMLS | C5680478 | 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 (2):
- ORPHA:101952Rare diabetes mellitus
rare endocrine diseases - ORPHA:183625Rare genetic diabetes mellitus
rare genetic diseases
Children (13):
- ORPHA:90301Acanthosis nigricans-insulin resistance-muscle cramps-acral enlargement syndrome
- ORPHA:79086Acquired generalized lipodystrophy
- ORPHA:280365Autosomal semi-dominant severe lipodystrophic laminopathy
- ORPHA:528Congenital generalized lipodystrophy
- ORPHA:508Donohue syndrome
- ORPHA:2297Insulin-resistance syndrome type A
- ORPHA:2298Insulin-resistance syndrome type B
- ORPHA:436144Intrauterine growth restriction-short stature-early adult-onset diabetes syndrome
- ORPHA:436182Microcephalic primordial dwarfism-insulin resistance syndrome
- ORPHA:280356PLIN1-related familial partial lipodystrophy
- ORPHA:769Rabson-Mendenhall syndrome
- ORPHA:3163SHORT syndrome
- ORPHA:66518Short fifth metacarpals-insulin resistance syndrome
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/181368
- This record as JSON: /data/d/181368.json