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Microcephaly 4, primary, autosomal recessive

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Description

Primary microcephaly (MCPH) is a clinical diagnosis made when an individual has a head circumference more than 3 standard deviations below the age- and sex-matched population mean and mental retardation, with no other associated malformations and with no apparent etiology. Most cases of primary microcephaly show an autosomal recessive mode of inheritance (summary by Woods et al., 2005). For a general phenotypic description and a discussion of genetic heterogeneity of primary microcephaly, see MCPH1 (251200).

OMIM

  • Mode of Inheritance

  • Autosomal recessive inheritance

VARIANTS

117

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Genes

External Links

  • OMIM

    604321

  • Orphanet
  • HPO
  • Medgen

    C1858516

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