ORPHA:179490
Obesity due to congenital leptin resistance
- Type
- Etiological subtype
- Group
- Subtype of disorder
- Status
- active
Orphadata ships no English definition for this code.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Obesity due to congenital leptin resistance | |
| fr | Obésité due à une résistance congénitale à la leptine | |
| de | Adipositas durch kongenitale Leptin-Resistenz | |
| es | Obesidad por resistencia congénita a la leptina | |
| it | Obesità da resistenza congenita alla leptina | |
| nl | Obesitas door congenitale leptineresistentie | |
| pt | Obesidade por resistência congénita à leptina | |
| pl | Otyłość spowodowana wrodzona opornością na leptynę | |
| cs | Obezita způsobená vrozenou rezistencí na leptin | |
| uk | Ожиріння через вроджену резистентність до лептину | |
| zh | 先天性瘦素抵抗所致肥胖 | |
| tr | Doğumsal leptin direncine bağlı obezite |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | E66.8 | NTBT | attributed | validated |
| ICD-11 | 5B81.Y | NTBT | index | validated |
| UMLS | C5680486 | 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:98267Genetic non-syndromic obesity
rare genetic diseases; rare endocrine diseases
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/179490
- This record as JSON: /data/d/179490.json