• LOC129933041 [Homo sapiens]
  LOC129933041 [Homo sapiens]

  Gene ID:129933041
  Gene
• Heterotaxy Syndrome
  Heterotaxy Syndrome

  Abnormal thoracoabdominal VISCERA arrangement (visceral heterotaxy) or malformation that involves additional CONGENITAL HEART DEFECTS (e.g., heart isomerism; DEXTROCARDIA) and...<br/>Year introduced: 2012
  MeSH
• Trichothiodystrophy Syndromes
  Trichothiodystrophy Syndromes

  Autosomal recessive neuroectodermal disorders characterized by brittle sulfur-deficient hair associated with impaired intellect, decreased fertility, and short stature. It may...<br/>Year introduced: 2008
  MeSH

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