Obesity due to CEP19 deficiency

Orpha code: 397615OMIM code: 615703

Definicja

A rare, genetic form of obesity characterized by morbid obesity, hypertension, type 2 diabetes mellitus and dyslipidemia leading to early coronary disease, myocardial infarction and congestive heart failure. Intellectual disability and decreased sperm counts or azoospermia have also been reported.

Disease data
Klasyfikacja

Etiological subtype

Kod ORPHA
397615
Kod OMIM
615703
Kod ICD10
E66.8
Kod ICD11
-

No additional description.

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