• Melanoma, cutaneous malignant, susceptibility to, 5
  Melanoma, cutaneous malignant, susceptibility to, 5
  MedGen
• Melanoma, cutaneous malignant, susceptibility to, 8
  Melanoma, cutaneous malignant, susceptibility to, 8
  MedGen
• Peutz-Jeghers Syndrome
  Peutz-Jeghers Syndrome

  A hereditary disease caused by autosomal dominant mutations involving CHROMOSOME 19. It is characterized by the presence of INTESTINAL POLYPS, consistently in the JEJUNUM, and...<br/>Year introduced: 1965
  MeSH
• trnW(uca) [Chondrilla aff. nucula CHOND]
  trnW(uca) [Chondrilla aff. nucula CHOND]

  Gene ID:5846846
  Gene
• FOXD4L5 forkhead box D4 like 5 [Homo sapiens]
  FOXD4L5 forkhead box D4 like 5 [Homo sapiens]

  Gene ID:653427
  Gene

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