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ENLymphatic Malformation 1 (LMPHM1)
Alias:
Milroy Disease
Hereditary Lymphedema Type I
Nonne-Milroy Lymphedema
Primary Congenital Lymphedema
Lymphedema, Hereditary, Type I, Formerly
Lymphedema, Hereditary, Ia, Formerly
Lymphedema, Early-Onset
Lmphm1
Pcl
Congenital Familial Lymphedema
Lymphatic Malformation, Type 1
Lymphedema Hereditary Type Ia
Lymphedema, Hereditary, 1a
Lymphedema Early-Onset
Lmph1a, Formerly
Milroy's Disease
Lmph1a
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Lymphatic Malformation 1, also known as milroy disease, is related to hereditary lymphedema i and hereditary lymphedema. An important gene associated with Lymphatic Malformation 1 is FLT4 (Fms Related Receptor Tyrosine Kinase 4), and among its related pathways/superpathways are Angiogenesis (CST) and Tyrosine Kinases / Adaptors. Affiliated tissues include skin and testis, and related phenotypes are lymphedema and hyperkeratosis
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MALACARDS
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MGI
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IF
