MeSH
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Syndrome, Gorlin

MeSH ID: T004295

Related Concepts:

  • Basal Cell Nevus Syndrome [M0002195]
    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.