Obesity due to leptin receptor gene deficiency

Orpha code: 179494OMIM code: 614963

Definition

A rare, genetic, non-syndromic, obesity disease characterized by severe, early-onset obesity, associated with major hyperphagia and endocrine abnormalities, resulting from leptin receptor deficiency.

Disease data
Classification

Etiological subtype

ORPHA code
179494
OMIM code
614963
ICD10 code
E66.8
ICD11 code
5B81.Y

No additional description.

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