Other obesity - CISMeF

Preferred Label : Other obesity;

Diag associé à un acte (%) : 79.3;

Diag pouvant être associé à un acte de chirurgie esthétique : true;

CODEXT : 1;

Source : OMS;

Date de début : 01/01/1997;

Date de mise à jour : 01/01/2017;

Do not code with : true;

Details

Origin ID

E668;

UMLS CUI

C0348480;

Orphanet concepts
- Genetic non-syndromic obesity [ORDO Disease]
- Genetic obesity [ORDO Disease]
- Obesity due MC3R deficiency [ORDO Disease]
- Obesity due to CEP19 deficiency [ORDO Disease]
- Obesity due to SIM1 deficiency [ORDO Disease]
- Obesity due to congenital leptin deficiency [ORDO Disease]
- Obesity due to congenital leptin resistance [ORDO Disease]
- Obesity due to leptin receptor gene deficiency [ORDO Disease]
- Obesity due to melanocortin 4 receptor deficiency [ORDO Disease]
- Obesity due to pro-opiomelanocortin deficiency [ORDO Disease]
- Obesity due to prohormone convertase I deficiency [ORDO Disease]
- Rapid-onset childhood obesity-hypothalamic dysfunction-hypoventilation-autonomic dysregulation syndrome [ORDO Disease]
- Severe early-onset obesity-insulin resistance syndrome due to SH2B1 deficiency [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Other Obesity [NCIt concept]

Keyword's position in hierarchy(ies) :

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