MeSH
HOME · CREATIVE · WEB · TECH · BLOG

Basal Cell Nevus Syndrome

MeSH ID: D001478

DEFINITION: Hereditary disorder consisting of multiple basal cell carcinomas, odontogenic keratocysts, and multiple skeletal defects, e.g., frontal and temporoparietal bossing, bifurcated and splayed ribs, kyphoscoliosis, fusion of vertebrae, and cervicothoracic spina bifida. Genetic transmission is autosomal dominant.

Related Concepts:

Qualifiers:

blood [Q000097] ; cerebrospinal fluid [Q000134] ; chemically induced [Q000139] ; classification [Q000145] ; complications [Q000150] ; diagnosis [Q000175] ; diet therapy [Q000178] ; drug therapy [Q000188] ; economics [Q000191] ; embryology [Q000196] ; enzymology [Q000201] ; epidemiology [Q000453] ; ethnology [Q000208] ; etiology [Q000209] ; genetics [Q000235] ; history [Q000266] ; immunology [Q000276] ; metabolism [Q000378] ; microbiology [Q000382] ; mortality [Q000401] ; nursing [Q000451] ; parasitology [Q000469] ; pathology [Q000473] ; physiopathology [Q000503] ; prevention & control [Q000517] ; psychology [Q000523] ; radiography [Q000530] ; radionuclide imaging [Q000531] ; radiotherapy [Q000532] ; rehabilitation [Q000534] ; surgery [Q000601] ; therapy [Q000628] ; ultrasonography [Q000736] ; ultrastructure [Q000648] ; urine [Q000652] ; veterinary [Q000662] ; virology [Q000821]

Tree Structure: