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MORM syndrome

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Description

Syndrome with the association of intellectual deficit, truncal obesity, retinal dystrophy and micropenis. It has been described in 14 individuals from a consanguineous family. It is transmitted in an autosomal recessive manner. The causative locus has been mapped to chromosome region 9q34.

SNOMEDCT_US

  • Mode of Inheritance

  • Autosomal recessive inheritance

VARIANTS

7

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Genes

External Links

  • OMIM

    610156

  • Orphanet

    75858

  • HPO
  • Medgen

    C1857802

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