• Homo sapiens ras homolog family member H (RHOH), transcript variant 6, mRNA
  Homo sapiens ras homolog family member H (RHOH), transcript variant 6, mRNA

  gi|1519244123|ref|NM_004310.5|
  Nucleotide
• Foot Deformities, Congenital
  Foot Deformities, Congenital

  Alterations or deviations from normal shape or size which result in a disfigurement of the foot occurring at or before birth.<br/>Year introduced: 1988
  MeSH
• Fraser Syndrome
  Fraser Syndrome

  Rare autosomal recessive congenital malformation syndrome characterized by cryptophthalmos, SYNDACTYLY and UROGENITAL ABNORMALITIES. Other anomalies of bone, ear, lung, and no...<br/>Year introduced: 2011
  MeSH

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