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

NCBI Reference Sequence: NM_004310.5

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  • 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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