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  • Gorlin syndrome Relevant markers:
    Frontal bossingHypertelorismMandibular prognathismDeformity of rib/s
    Parents markers:
    MacrocephalyAgenesis of corpus callosum (ACC)VentriculomegalyCleft lipCleft in hard palateScoliosisVertebral body
      Incidence:1/57000 — -
      Male — Female Ratio:1 — 1
      Involved genes:
      (gene — definition — chromosome)      		PTCH1 — 9q22.32, PTCH2 — 1p32, SUFU — 10q2-q25
      Inheritance mode:AD
      Other online databases:OrphaNet, OMIM, Geneva Foundation, Jablonski's Database
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