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GTR Home > Conditions/Phenotypes > Obesity due to CEP19 deficiency

Obesity due to CEP19 deficiency

Synonyms
Morbid obesity and spermatogenic failure
Modes of inheritance
Autosomal recessive inheritance (Orphanet)

Summary

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. [from ORDO]

Available tests

9 tests are in the database for this condition.

Check Related conditions for additional relevant tests.

Clinical tests (9 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

  • Also known as: C3orf34, MOSPGF, CEP19
    Summary: centrosomal protein 19

Clinical features

Help
Imported from Human Phenotype Ontology (HPO)

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