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Lymphatic malformation 7

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Description

LMPHM7 is an autosomal dominant disorder with variable expressivity. Some patients may develop severe nonimmune lymphatic-related hydrops fetalis (LRHF) in utero, resulting in early death, whereas others may have milder manifestations, such as atrial septal defect (ASD) or varicose veins as adults. The hydrops and/or swelling improves spontaneously in those who survive the neonatal period (summary by Martin-Almedina et al., 2016). For a discussion of genetic heterogeneity of lymphatic malformation, see 153100.

OMIM

  • Mode of Inheritance

  • Autosomal dominant inheritance

VARIANTS

9

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Genes

External Links

  • OMIM

    617300

  • Orphanet
  • HPO
  • Medgen

    C4310629

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